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Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/1997, Volume 99, Issue 8, pp. 1897 - 1905
Mutations in the arginine vasopressin (AVP) gene cause autosomal dominant familial neurohypophyseal diabetes insipidus (FNDI). The dominant inheritance pattern... 
genetic mutation | neurohypophyseal diabetes insipidus | neuronal toxicity | autosomal dominant inheritance | endoplasmic reticulum | SIGNAL | MEDICINE, RESEARCH & EXPERIMENTAL | BOVINE NEUROPHYSIN-II | NEUROBLASTOMA-CELLS | ARGININE-VASOPRESSIN | TRANSPORT | GENE | K QA MEDICINE, RESEARCH & EXPERIMENTAL | CODING REGION | MUTATION | LIVER | TRANSGENIC MICE
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