Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy-Reference-Cited by-同舟云学术

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy

Published:2000-12 Issue:8 Volume:10 Page:572-577
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Kerst Birgit,Mennerich Detlev,Schuelke Markus,Stoltenburg-Didinger Gisela,von Moers Arpad,Gossrau Reinhart,van Landeghem Frank K.H,Speer Astrid,Braun Thomas,Hübner Christoph

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference32 articles.

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4. Crystal structure of MyoD bHLH domain-DNA complex: perspectives on DNA recognition and implications for transcriptional activation;Ma;Cell,1994

5. Skeletal muscle determination and differentiation: story of a core regulatory network and its context;Yun;Curr Opin Cell Biol,1996

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