AP4S1 splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyria
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Article Information
- Received February 20, 2018
- Accepted in final form July 31, 2018
- First Published September 19, 2018.
Author Disclosures
- Susana Carmona, PhD,
- Clara Marecos, MD,
- Marta Amorim, MD,
- Ana C. Ferreira, MD,
- Carla Conceição, MD,
- José Brás, PhD,
- Sofia T. Duarte, MD, PhD* and
- Rita Guerreiro, PhD*
- Susana Carmona, PhD,
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- Clara Marecos, MD,
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- Marta Amorim, MD,
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- Ana C. Ferreira, MD,
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- Carla Conceição, MD,
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- José Brás, PhD,
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Journal of Parkinson's disease, editorial board member, 2017
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Alzheimer's Society
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- Sofia T. Duarte, MD, PhD* and
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Nutricia, Travel
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- Rita Guerreiro, PhD*
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(1) Science Matters, Editorial board, from 2016, (2) American Journal of Neurodegenerative Disease, Associate Editorial board, from 2012, (3) Editorial Board Member of Journal of Parkinson?s Disease
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Alzheimer's Society
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- From the Department of Molecular Neuroscience (S.C., J.B., R.G.), UCL Institute of Neurology, University College London, United Kingdom; Paediatric Neurology Department (C.M., S.T.D.), Hospital Dona Estefânia, Centro Hospitalar de Lisboa Central; Genetics Department (M.A.), Hospital Dona Estefânia, Centro Hospitalar de Lisboa Central; Reference Center of Inherited Metabolic Diseases (A.C.F.), Centro Hospitalar de Lisboa Central; Neuroradiology Department (C.C.), Hospital Dona Estefânia, Centro Hospitalar de Lisboa Central, Lisbon, Portugal; UK Dementia Research Institute (J.B., R.G.), University College London, United Kingdom; and Department of Medical Sciences (J.B., R.G.), Institute of Biomedicine, iBiMED, University of Aveiro, Portugal.
- Correspondence
Dr. Guerreiro r.guerreiro{at}ucl.ac.uk
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