A single base substitution in the coding region for neurophysin II associated with familial central diabetes insipidus.

To elucidate the molecular mechanism of familial central diabetes insipidus (FDI), we sequenced the arginine vasopressin-neurophysin II (AVP-NPII) gene in 2 patients belonging to a pedigree that is consistent with an autosomal dominant mode of inheritance. 10 patients with idiopathic central diabete...

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Main Authors: Ito, M, Mori, Y, Oiso, Y, Saito, H
Formato: Artigo
Idioma:Inglês
Publicado: 1991
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC296365/
https://ncbi.nlm.nih.gov/pubmed/1840604
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