Facioscapulohumeral dystrophy: activating an early embryonic transcriptional program in human skeletal muscle-Reference-Cited by-同舟云学术

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Facioscapulohumeral dystrophy: activating an early embryonic transcriptional program in human skeletal muscle

Published:2018-04-28 Issue:R2 Volume:27 Page:R153-R162
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Campbell Amy E¹,Belleville Andrea E¹,Resnick Rebecca¹²³,Shadle Sean C¹²,Tapscott Stephen J¹⁴

Affiliation:

1. Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA

2. Molecular and Cellular Biology Program, University of Washington, Seattle, WA, USA

3. Medical Scientist Training Program, University of Washington, Seattle, WA, USA

4. Department of Neurology, University of Washington, Seattle, WA, USA

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/R2/R153/25229880/ddy162.pdf

Reference121 articles.

1. Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy;Flanigan;Neuromuscul. Disord,2001

2. Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample;Mostacciuolo;Clin. Genet,2009

3. Population-based incidence and prevalence of facioscapulohumeral dystrophy;Deenen;Neurology,2014

4. Diagnostic criteria for facioscapulohumeral muscular dystrophy;Padberg;Neuromuscul. Disord,1991

5. Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data;Goselink;Neuromuscul. Disord,2017

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