Lower limb muscle strength impairment in late-onset and adult myotonic dystrophy type 1 phenotypes

Author:

Petitclerc Émilie1,Hébert Luc J.2,Mathieu Jean1,Desrosiers Johanne1,Gagnon Cynthia1

Affiliation:

1. Faculty of Medicine and Health Sciences; Université de Sherbrooke; Sherbrooke Québec Canada

2. Faculty of Medicine, Rehabilitation (Physiotherapy) and Radiology Department; Université Laval; Québec City Québec Canada

Funder

Corporation de recherche et d'action sur les maladies héréditaires

Université de Sherbrooke

Foundation Go

Ordre professionnel de la physiothérapie du Québec

Groupe de recherche interdisciplinaire sur les maladies neuromusculaires. C.G. holds a career grant from Fonds de Recherche du Québec-Santé

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference27 articles.

1. Towards an integrative approach to the management of myotonic dystrophy type 1;Gagnon;J Neurol Neurosurg Psychiatry,2007

2. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy;Harley;Am J Hum Genet,1993

3. New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1);International Myotonic Dystrophy Consortium;Neurology,2000

4. Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions;Arsenault;Neurology,2006

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