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A Double-Point Mutation in the Selectivity Filter Site of the KCNQ1 Potassium Channel Results in a Severe Phenotype, LQT1, of Long QT Syndrome
TARUNA IKRAR, HARUO HANAWA, HIROSHI WATANABE, SHINSUKE OKADA, YOSHIYASU AIZAWA, MAHMOUD M. RAMADAN, SATORU KOMURA, FUMIO YAMASHITA, MASAOMI CHINUSHI, YOSHIFUSA AIZAWAVolume:
19
Year:
2008
Language:
english
Pages:
9
DOI:
10.1111/j.1540-8167.2007.01076.x
File:
PDF, 2.41 MB
english, 2008