Open AccessFamilial Corticosteroid-Binding Globulin Deficiency Due to a Novel Null Mutation: Association with Fatigue and Relative Hypotension
Author(s) -
David J. Torpy
Publication year - 2001
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.86.8.3692
Subject(s) - transcortin , heterozygote advantage , endocrinology , null allele , medicine , globulin , corticosteroid , mutation , blood pressure , biology , allele , genetics , gene
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