Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus.
Repaske, D R; Summar, M L; Krishnamani, M R; Gültekin, E K; Arriazu, M C; Roubicek, M E; Blanco, M; Isaac, G B; Phillips, J A
- 期刊名称The Journal of Clinical Endocrinology & Metabolism
- 作者Repaske, D R; Summar, M L; Krishnamani, M R; Gültekin, E K; Arriazu, M C; Roubicek, M E; Blanco, M; Isaac, G B; Phillips, J A
- 卷第81卷
- 期第6期
- 印刷ISSN0021-972X
- 电子ISSN1945-7197
- 文件大小1188.72KB
- 发表时间1996-06
- DOI10.1210/jcem.81.6.8964872
- 页码2328-2334