Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency
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Article Information
- Received May 17, 2017
- Accepted in final form September 29, 2017
- First Published December 18, 2017.
Author Disclosures
- Rabah Ben Yaou, MD*,
- Aurélie Hubert, PhD*,
- Isabelle Nelson, PhD,
- Julia R. Dahlqvist, MD,
- David Gaist, MD, PhD,
- Nathalie Streichenberger, MD,
- Maud Beuvin, BS,
- Martin Krahn, MD, PhD,
- Philippe Petiot, MD,
- Frédéric Parisot, BS,
- Fabrice Michel, MD,
- Edoardo Malfatti, MD, PhD,
- Norma Romero, MD,
- Robert Yves Carlier, MD, PhD,
- Bruno Eymard, MD, PhD,
- Philippe Labrune, MD, PhD,
- Morten Duno, PhD,
- Thomas Krag, PhD,
- Mathieu Cerino, PharmD,
- Marc Bartoli, PhD,
- Gisèle Bonne, PhD,
- John Vissing, MD, PhD*,
- Pascal Laforet, MD, PhD* and
- François M. Petit, PharmD, PhD*
- Rabah Ben Yaou, MD*,
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- Aurélie Hubert, PhD*,
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- Isabelle Nelson, PhD,
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- Julia R. Dahlqvist, MD,
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- David Gaist, MD, PhD,
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Received honoraria from AstraZeneca (Sweden) for participation as a co-investigator in a research project.
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Received research grant from Danish Cancer Society (grant nr. R56-A2879)
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- Nathalie Streichenberger, MD,
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- Maud Beuvin, BS,
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- Martin Krahn, MD, PhD,
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Cahiers de Myologie, editorial board
(1) - ?Exon-skipping for dysferlinopathies therapy? (2)- ?In vitro genetic diagnostic of inherited neuromuscular disorders?
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Ultragenyx
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(1) European Community Seventh Framework Program (Grant Agreement No. 2012?305121) ?Integrated European omics research project for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases? (NEUROMICS).
(1) INSERM recurent funding
(1) AFM-TELETHON 2016-2021
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- Philippe Petiot, MD,
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- Frédéric Parisot, BS,
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- Fabrice Michel, MD,
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- Edoardo Malfatti, MD, PhD,
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Frontiers in Neurology, Associate Editor, 2015-
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- Norma Romero, MD,
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- Robert Yves Carlier, MD, PhD,
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Speaker honoraria by Genzyme corporation for “step forwards in Pompe disease” and Fabry summer school
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- Bruno Eymard, MD, PhD,
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conferences for LFB, Biogen and BioMarin companies
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AFM (Association Fran?aise contre les myopathies)
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- Philippe Labrune, MD, PhD,
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- Morten Duno, PhD,
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- Thomas Krag, PhD,
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(1) AP M?ller Foundations, (2) Augustinus Foundation, (3) Danielsen Foundation.
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- Mathieu Cerino, PharmD,
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- Marc Bartoli, PhD,
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- Gisèle Bonne, PhD,
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(1) Journal of Neuromuscular Diseases, Associate Editor, 2014, (2) Neuromuscular Disorders, Editorial Board Member, 2007-2014
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-ANR French-German grant (ANR-BMBF)
1) Association Institut de Myologie (AIM) 2) GIS Maladies Rares ?Plateforme Mutations? 3) CURE-CMD Translational Award
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- John Vissing, MD, PhD*,
On the advisory board Sanofi/Genzyme, aTyr pharma, Ultragenyx Pharmaceuticals, Santhera Pharmaceuticals, Sarepta Therapeutics, NOVO Nordisk, Alexion Pharmaceuticals and Stealth Biotherapeutics
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travel and speaker honoraria from Sanofi/Genzyme, Alexion Pharmaceuticals, Ultragenyx Pharmaceuticals, Santhera Pharmaceuticals and aTyr Pharma
Editorial Board member for the journals, Neuromuscular Disorders and Journal of Neuromuscular Diseases.
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Grants from Lundbeck Foundation, NOVO foundation
Danish Medical Research Council, University of Copenhagen, The research Committee of the National Hopsital
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- Pascal Laforet, MD, PhD* and
I am member of Genzyme-Sanofi Pompe advisory board
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I received funding for travel and speaker honoraria form Genzym-Sanofi
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I received research supports from Genzyme-Sanofi for the French Pompe Registry, and from Valerion Therapeutics to support the Glycogenosis type III registry
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I received fundings from French Glycogenosis Association
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- François M. Petit, PharmD, PhD*
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- From the Assistance Publique-Hôpitaux de Paris (APHP) (R.B.Y., B.E., P.L.), Groupe Hospitalier Universitaire la Pitié-Salpêtrière, Centre de Référence de Pathologie Neuromusculaire Paris-Est, Institut de Myologie; Sorbonne Universités (R.B.Y., I.N., M.B., G.B.), UPMC Université Paris 06, INSERM UMRS 974, Center of Research in Myology, Institut de Myologie, Paris; Department of Molecular Genetics (A.H., F.P., F.M.P.), Assistance Publique-Hôpitaux de Paris (APHP), Hôpitaux Universitaires Paris Sud, Antoine Béclère Hospital, Clamart; Department of Pediatrics (A.H., P.L.), Assistance Publique-Hôpitaux de Paris (APHP), Hôpitaux Universitaires Paris Sud, Antoine Béclère Hospital, Referal Center for Metabolic Liver Inherited Diseases, Clamart, and Université Paris-Sud, France; Department of Neurology (J.R.D., T.K., J.V.), Copenhagen Neuromuscular Center, Rigshospitalet, University of Copenhagen; Department of Neurology (D.G.), Odense University Hospital, Denmark; Hospices Civils de Lyon (N.S.), Groupement Hospitalier Est, Centre de Pathologie et Neuropathologie Est, Service de Neuropathologie, Université Claude-Bernard Lyon 1, CNRS UMR5239, LBMC, ENS; AP-HM, Département de Génétique Médicale (M.K., M.C., M.B.), Hôpital Timone Enfants; Aix Marseille Université (M.K., M.C., M.B.), Inserm, GMGF, UMR_S910; Hospices Civils de Lyon (P.P.), Hôpital la Croix-Rousse, Département de Neurologie, Université Claude Bernard Lyon 1; CHU Besançon (F.M.), Hôpital Jean Minjoz, Centre de Référence de Pathologie Neuromusculaire; Unité de morphologie neuromusculaire (E.M., N.R.), Groupe Hospitalier Universitaire La Pitié-Salpêtrière; Sorbonne Universités UPMC Université Paris 06; Assistance Publique-Hôpitaux de Paris (APHP) (R.Y.C.), Service d'imagerie Médicale, CIC-IT Handicap, Hôpital Raymond Poincaré, Garches, France; and Department of Clinical Genetics (M.D.), Rigshospitalet, University of Copenhagen, Denmark.
- Correspondence to Dr. Petit: francois.petit2{at}aphp.fr
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