Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin–neurophysin II gene

✍ Scribed by Luo, Yongfeng; Wang, Binbin; Qiu, Yu; Zhang, Chuan; Jin, Chengluo; Zhao, Yakun; Zhu, Qingguo; Ma, Xu

• Book ID: 113093194
• Publisher: Springer
• Year: 2012
• Tongue: English
• Weight: 268 KB
• Volume: 42
• Category: Article
• ISSN: 0969-711X
• DOI: 10.1007/s12020-012-9606-2