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Two novel mutations of the vasopressin gene associated with familial diabetes insipidus and identification of an asymptomatic carrier infant

Autor: F D, Grant, A, Ahmadi, C M, Hosley, J A, Majzoub

Publikováno v: The Journal of clinical endocrinology and metabolism. 83(11)

Familial diabetes insipidus (FDI) is a syndrome of central vasopressin deficiency that is inherited in an autosomal dominant manner and that typically becomes clinically apparent in the first decade of life. Two novel mutations of the vasopressin gen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::61612ec0e90448672aa53c8646171181
https://pubmed.ncbi.nlm.nih.gov/9814475

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