(Q77313509)
Statements
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 (English)
Yamagishi H
Furutani M
Kamisago M
Morikawa Y
Kojima Y
Hino Y
Furutani Y
Kimura M
Imamura S
Takao A
Momma K
1 January 1998