The novel compound heterozygous mutations, V434del and...

Endocrine (Springer) 2009 / 04 Vol. 35; Iss. 2

The novel compound heterozygous mutations, V434del and W666X, inWFS1gene causing the Wolfram syndrome in a Chinese family

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
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Volume:
35
Language:
english
Pages:
7
Journal:
Endocrine
DOI:
10.1007/s12020-009-9145-7
Date:
April, 2009
File:
PDF, 489 KB
english, 2009
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