A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT sydrome. Mutations in brief no. 140. Online.

H. Yamagishi, M. Furutani, M. Kamisago, Y. Morikawa, Y. Kojima, Y. Hino, Y. Furutani, M. Kimura, S. Imamura, A. Takao, K. Momma, R. Matsuoka

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