Suchergebnisse - (Person:"Gao, Ya")

PubPharm (2)

1

A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family

enthalten in: Human genetics | 2003

von Qi, Y. | Jia, H. | Huang, S. | +8

2

A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family

enthalten in: Human genetics | 2003

von Qi, Y. | Jia, H. | Huang, S. | +8

1
[1]