Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophy-Reference-Cited by-同舟云学术

Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophy

Published:2015-10-28 Issue:7 Volume:58 Page:698-705
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Johnson Nicholas E¹,Ekstrom Anne-Berit²,Campbell Craig³,Hung Man⁴⁵,Adams Heather R⁶,Chen Wei⁵,Luebbe Elizabeth⁶,Hilbert James⁶,Moxley Richard T⁶,Heatwole Chad R⁶

Affiliation:

1. Department of Neurology; The University of Utah; Salt Lake City UT USA

2. Department of Pediatrics; The Queen Silvia Children's Hospital; Sahlgrenska Academy at the University of Gothenburg; Gothenburg Sweden

3. Department of Neurology; London Health Science Centre; London ON Canada

4. Department of Orthopedics; The University of Utah; Salt Lake City UT USA

5. Division of Epidemiology; The University of Utah; Salt Lake City UT USA

6. Department of Neurology; The University of Rochester; Rochester NY USA

Funder

Myotonic Dystrophy Foundation

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/dmcn.12948/fullpdf

Reference25 articles.

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

2. Myotonic dystrophy mutation: an unstable CTG repeat in the 3’ untranslated region of the gene;Mahadevan;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. Genetic risks for children of women with myotonic dystrophy;Koch;Am J Hum Genet,1991

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