Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10; 17) may indicate candidate gene regions
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb03982.x/fullpdf
Reference29 articles.
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2. Progressive myopathy in hyperkalemic periodic paralysis;Bradley;Arch Neurol,1990
3. Opening the gates on ion channel diseases;Caldwell;Nature Genet,1992
4. Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook;Cavanagh;Arch Dis Child,1979
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