Familial Atrial Septal Defect and Atrioventricular Conduction Disturbance Associated With a Point Mutation in the Cardiac Homeobox Gene CSX/NKX2-5 in a Japanese Patient
Journal article published in 1999 by
Toru Hosoda 
,
Issei Komuro,
Ichiro Shiojima,
Yukio Hiroi,
Miki Harada,
Yuji Murakawa,
Yasunobu Hirata,
Yoshio Yazaki
,
Issei Komuro,
Ichiro Shiojima,
Yukio Hiroi,
Miki Harada,
Yuji Murakawa,
Yasunobu Hirata,
Yoshio Yazaki
This paper is made freely available by the publisher.
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