Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family
Ke, Tie, Gomez, Cladelis Rubio, Mateus, Heidi Eliana, Castano, Juan Andres, Wang, Qing KennethVolume:
54
Language:
english
Journal:
Journal of Human Genetics
DOI:
10.1038/jhg.2009.92
Date:
November, 2009
File:
PDF, 329 KB
english, 2009