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

Journal of Clinical Endocrinology and Metabolism

Volumn 83, Issue 11, 1998, Pages 3958-3964

  Grant, Frederick D ^a,b,d   Ahmadi, Arshanoush ^c   Hosley, Catherine M ^a   Majzoub, Joseph A ^b,d  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NEUROPHYSIN; VASOPRESSIN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; DIABETES INSIPIDUS; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HETEROZYGOTE; HUMAN; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; WATER DEPRIVATION;

EID: 0031732499     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.83.11.3958     Document Type: Article

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