The novel compound heterozygous mutations, V434del and W666X, in WFS1 gene causing the Wolfram syndrome in a Chinese family

Verfasser / Beitragende:
[Jie Hong, Yu-wen Zhang, Hui-Jie Zhang, Hui-ying Jia, Yu Zhang, Xiao-yi Ding, Dan-yang Zhou, Hui-ping Chen, Xiao-hua Jiang, Bin Cui, Xiao-ying Li, Guang Ning]
Ort, Verlag, Jahr:
2009
Enthalten in:
Endocrine, 35/2(2009-04-01), 151-157
Format:
Artikel (online)
ID: 453622623