Physical function and mobility in children with congenital myotonic dystrophy-Reference-Cited by-同舟云学术

Physical function and mobility in children with congenital myotonic dystrophy

Published:2017-02-13 Issue:2 Volume:56 Page:224-229
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Pucillo Evan M.¹,Dibella Deanna L.¹,Hung Man²³,Bounsanga Jerry²,Crockett Becky¹,Dixon Melissa¹,Butterfield Russell J.⁴,Campbell Craig⁵,Johnson Nicholas E.¹

Affiliation:

1. Eccles Institute of Human Genetics, Department of Neurology; University of Utah School of Medicine; 15N 2030 East Salt Lake City Utah 84112 USA

2. Department of Orthopedics; University of Utah; Salt Lake City Utah USA

3. Division of Public Health; University of Utah; Salt Lake City Utah USA

4. Department of Pediatrics; University of Utah; Salt Lake City Utah USA

5. Department of Pediatrics, Clinical Neurological Sciences and Epidemiology; Western University; London Ontario Canada

Funder

National Institutes of Health

Muscular Dystrophy Association

Valerion Therapeutics

Utah Neuromuscular Research Fund

Quality Outcomes Research and Assessment

Study Design and Biostatistics Center

Publisher

Wiley

Subject

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

Reference34 articles.

1. Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene;Mahadevan;Science,1992

2. An unstable triplet repeat in a gene related to myotonic muscular dystrophy;Fu;Science,1992

3. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992

4. Orthopaedic manifestations of congenital myotonic dystrophy during childhood and adolescence;Canavese;J Pediatr Orthop,2009

5. Dystrophia myotonica in childhood;Vanier;BMJ,1960

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