Author:
Reilly Mary M.,Pareyson Davide,Burns Joshua,Laurá Matilde,Shy Michael E.,Singh Dishan,Agren Per Henrik,Altmann Viola,Baets Jonathan,Briggs Peter,Burns Joshua,Butcher Karen,Gaiani Luca,Genovese Filippo,Gibbons Paul,Laurá Matilde,Louwerens Jan Willem,Manzur Adnan,Moroni Isabella,Martinelli Nicolò,Pareyson Davide,Pfeffer Glenn,Ramdharry Gita,Reilly Mary M.,Shy Michael,Singh Dishan,van der Linden Marco,Wenz Wolfram
Funder
European Neuromuscular Centre
Association Française contre les Myopathies
Deutsche Gesellschaft für Muskelkranke
Muscular Dystrophy UK, Muskelsvindfonden
Prinses Beatrix Spierfonds
Schweizerische Stiftung für die Erforschung der Muskelkrankheiten
Telethon Foundation
Spierziekten Nederland
Finnish Neuromuscular Association
CMTUK
National Institutes of Neurological Diseases and Stroke and office of Rare Diseases
INC
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference11 articles.
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4. Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype;Hoogendijk;Muscle Nerve,1994
5. Charcot-Marie-Tooth disease in northern Sweden: an epidemiological and clinical study;Holmberg;Acta Neurol Scand,1993
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