论文信息 - 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. - 字舞流文

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.

Y. Hiroi | Y. Yazaki | I. Komuro | I. Shiojima | M. Harada | Y. Hirata | T. Hosoda | Y. Murakawa | I. Komuro | Y. Hirata | T. Hosoda | Y. Yazaki | Miki Harada