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An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity
Takano, K., Liu, D., Tarpey, P., Gallant, E., Lam, A., Witham, S., Alexov, E., Chaubey, A., Stevenson, R. E., Schwartz, C. E., Board, P. G., Dulhunty, A. F.Volume:
21
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/dds292
Date:
October, 2012
File:
PDF, 387 KB
english, 2012