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Isolated growth hormone deficiency due to the R183H mutation in GH 1 : Clinical analysis of a four‐generation family
Author(s) -
CabreraSalcedo Catalina,
Shah Amy S.,
Andrew Melissa,
Tyzinski Leah,
Hwa Vivian,
GutmarkLittle Iris,
Backeljauw Philippe,
Dauber Andrew
Publication year - 2017
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1111/cen.13400
Subject(s) - mutation , endocrinology , medicine , growth hormone , hormone , genetics , biology , gene
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