BAG3-related myofibrillar myopathy in a Chinese family
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01659.x/fullpdf
Reference26 articles.
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2. Mutation in BAG3 causes severe dominant childhood muscular dystrophy.;Selcen;Ann Neurol,2009
3. Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation.;Odgerel;Neuromuscul Disord,2010
4. An evolutionarily conserved family of Hsp70/Hsc70 molecular chaperone regulators.;Takayama;J Biol Chem,1999
5. BAG3 and Hsc70 interact with actin capping protein CapZ to maintain myofibrillar integrity under mechanical stress.;Hishiya;Circ Res,2010
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