CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis
Citation Manager Formats
Make Comment
See Comments

Article Information
- Received October 19, 2016
- Accepted in final form February 6, 2017
- First Published March 22, 2017.
Author Disclosures
- Holger Hengel, MD*,
- Alex Magee, MD*,
- Muhammad Mahanjah, MD*,
- Jean-Michel Vallat, MD,
- Robert Ouvrier, MD,
- Mohammad Abu-Rashid, MD,
- Jamal Mahamid, MD,
- Rebecca Schüle, MD,
- Martin Schulze, PhD,
- Ingeborg Krägeloh-Mann, MD,
- Peter Bauer, MD,
- Stephan Züchner, MD,
- Rajech Sharkia, PhD and
- Ludger Schöls, MD
- Holger Hengel, MD*,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Alex Magee, MD*,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Muhammad Mahanjah, MD*,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Jean-Michel Vallat, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
French Minister of Health as a reference center for rare peripheral neuropathies : 2006 to 2011
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Robert Ouvrier, MD,
I am on the scientific Advisory Board of the Nerve Foundation of the University of Sydney and of the Institute for Neuromuscular Research at The Children's Hospital at Westmead, Sydney. Both are non-profit bodies from which I receive no recompense.
NONE
NONE
(1) Editorial advisory board member: Brain and Development for approximately twenty years
NONE
I receive royalties of less than US$100 annually from MacKeith Press, London UK for a book entitled
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Mohammad Abu-Rashid, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Jamal Mahamid, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Rebecca Schüle, MD,
(2) Scientific advisory board for Viagenetics
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
European Union, PIOF-GA-2012-326681European Union, 01GM1408BNIH, 2R01NS072248-06A1
NONE
HSP Selbsthilfegruppe e.V.Spastic Paraplegia FoundationEva Luise und Horst K?hler Stiftung
NONE
NONE
NONE
NONE
NONE
NONE
- Martin Schulze, PhD,
NONE
NONE
NONE
NONE
NONE
NONE
(1)Praxis f?r Humangenetik T?bingen, scientist indiagnostic service, 0.5 years(2) CeGaT T?bingen, scientist in diagnostic service, 0.5 years
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Ingeborg Krägeloh-Mann, MD,
intrathecal enzyme replacement in metachromaticleukodystrophy - phase I/II study startingShire 2012
NONE
NONE
Developmental medicine and child neurology since 2006Neuropediatrics since 2000European Journal of Paediatric Neurology since 2009
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
German Research CouncilDFGSFB 833 B05KSyntax and Semantics of Reorganized Languageand its Neuronal Architecture7/2010-6/2013SCPE-Net DGXII-BIOMED2BMH4-983701-QLG5-CT-2001.30133Surveillance in CerebralPalsy in Europe4/2002-12/2011Leukonet 01 GM030901 GM0644Childhood leukodystrophies with known geneticdefect11/2003-12/2011Leukonet01 GM0835Netzwerk Leukodystrophien12/2008-12/2012Leukotreat FP7-HEALTH-F2 2010-241622
NONE
Brains for BrainDeveloping treatment options for Metachromatic Leukodystrophy2010-2012
NONE
NONE
NONE
NONE
NONE
NONE
- Peter Bauer, MD,
(1) Scientific advisory board for ZOOM study, ActelionPharmaceuticals, Allschwil, CH
NONE
(1) Speaker honoraria from Actelion Pharmaceuticals,Allschwil, CH
NONE
NONE
NONE
NONE
(1) Consultant for Actelion Pharmaceuticals, Allschwil, CH(2) Consultant for CENTOGENE AG, Rostock, GER
NONE
NONE
NONE
NONE
(1) German Research Council (BMBF) to GeNeMove (01GM0603),EUROSPA (01GM0807) and RISCA (09GM0820)(2) EU for EUROSCA (LSHM-CT-2004-503304), MarkMD(FP7-People PIAP-2008-230596) and TECHGENE (FP7-Health2007-B 223143).
NONE
NONE
(1) Centogene AG, Rostock, Germany
NONE
(1) Improved DNase treatment protocol, Roche, Mannheim, GER
NONE
NONE
NONE
- Stephan Züchner, MD,
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Rajech Sharkia, PhD and
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
- Ludger Schöls, MD
NONE
NONE
(1) Speaker honorar from Actelion
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
NONE
I received the following grants:PI: Genetic disorders in Arab Societies (grantSCHO754/5-2), DFG: 2014-2017PI: NEUROMICS (F5-2012-305121) EU: 2012-2017
NONE
I received additional funding from theHSP-Selbsthilfegruppe Deutschland eV and the F?rdervereinfuer HSP-Forschung
NONE
NONE
NONE
NONE
NONE
NONE
- From the Department of Neurology and Hertie-Institute for Clinical Brain Research (H.H., R. Schüle, L.S.), University of Tübingen, Germany; German Center of Neurodegenerative Diseases (DZNE) (H.H., R.S., L.S.), Tübingen, Germany; Northern Ireland Regional Genetics Service (A.M.), Belfast City Hospital, Belfast; Department of Neurology (J.-M.V.), National Reference Center for Rare Peripheral Neuropathies, University Hospital, Limoges, France; Institute for Neuroscience and Muscle Research (R.O.), The Children's Hospital at Westmead, Sydney, New South Wales, Australia; The Triangle Regional Research and Development Center (R. Sharkia), Kfar Qari' Israel; Beit-Berl Academic College (R. Sharkia), Israel; Child Neurology and Development Center (M.M.), Hillel-Yaffe Medical Center, Hadera, Israel; Rappaport Faculty of Medicine (M.M.), Technion, Haifa, Israel; Institute of Medical Genetics and Applied Genomics (M.S.), University of Tübingen, Germany; Department of Pediatric Neurology (I.K.-M.), University Medical Center Tübingen, Germany; Hussman Institute for Human Genomics (S.Z.), University of Miami Miller School of Medicine, FL; Clalit Health Services (M.A.-R.), Haifa, Israel; and Meuhedet Health Services (J.M.), North District, Israel.
- Correspondence to Dr. Schöls: Ludger.Schoels{at}uni-tuebingen.de
Article usage
Cited By...
Letters: Rapid online correspondence
REQUIREMENTS
You must ensure that your Disclosures have been updated within the previous six months. Please go to our Submission Site to add or update your Disclosure information.
Your co-authors must send a completed Publishing Agreement Form to Neurology Staff (not necessary for the lead/corresponding author as the form below will suffice) before you upload your comment.
If you are responding to a comment that was written about an article you originally authored:
You (and co-authors) do not need to fill out forms or check disclosures as author forms are still valid
and apply to letter.
Submission specifications:
- Submissions must be < 200 words with < 5 references. Reference 1 must be the article on which you are commenting.
- Submissions should not have more than 5 authors. (Exception: original author replies can include all original authors of the article)
- Submit only on articles published within 6 months of issue date.
- Do not be redundant. Read any comments already posted on the article prior to submission.
- Submitted comments are subject to editing and editor review prior to posting.
You May Also be Interested in
Dr. Babak Hooshmand and Dr. David Smith
► Watch
Related Articles
- No related articles found.
Topics Discussed
Alert Me
Recommended articles
-
Article
Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa AnomaliesLior Greenbaum, Idit Maya, Lena Sagi-Dain et al.Neurology: Genetics, May 28, 2021 -
Articles
Longitudinal MRI findings in pyridoxine-dependent seizuresSidney M. Gospe, Jr., Stephen T. Hecht et al.Neurology, July 01, 1998 -
Article
Pontocerebellar hypoplasia type 1Clinical spectrum and relevance of EXOSC3 mutationsSabine Rudnik-Schöneborn, Jan Senderek, Joanna C. Jen et al.Neurology, January 02, 2013 -
Articles
A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposisE. Kimber, H. Tajsharghi, A. -K. Kroksmark et al.Neurology, August 21, 2006