Patient‐reported study of the impact of pediatric‐onset myotonic dystrophy-Reference-Cited by-同舟云学术

Patient‐reported study of the impact of pediatric‐onset myotonic dystrophy

Published:2019-07-26 Issue:4 Volume:60 Page:392-399
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Hunter Michael¹,Ekstrom Anne‐Berit²,Campbell Craig³,Hung Man⁴,Bounsanga Jerry⁵,Bates Kameron⁶,Adams Heather R.⁷,Luebbe Elizabeth⁷,Moxley Richard T.⁷,Heatwole Chad⁷,Johnson Nicholas E.⁶^ORCID

Affiliation:

1. Department of NeurologyUniversity of Utah School of Medicine Salt Lake City Utah

2. Regional Pediatric Rehabilitation CenterQueen Silvia Children's Hospital Gothenburg Sweden

3. Department of Pediatrics, Epidemiology and Clinical NeurologyUniversity of Western Ontario, London Health Science Centre London Ontario Canada

4. College of Dental Medicine, Roseman University of Health Sciences Henderson Nevada

5. Department of Public HealthUniversity of Utah Salt Lake City Utah

6. Department of NeurologyVirginia Commonwealth University Richmond Virginia

7. Department of NeurologyUniversity of Rochester Rochester New York

Funder

Myotonic Dystrophy Foundation

National Institute of Arthritis and Musculoskeletal and Skin Diseases

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.26632

Reference28 articles.

1. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy

2. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene

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

4. Genetic risks for children of women with myotonic dystrophy;Koch MC;Am J Hum Genet.,1991

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