Open AccessA missense mutation in the second transmembrane segment of the luteinizing hormone receptor causes familial male-limited precocious puberty
Author(s) -
R. Kraaij
Publication year - 1995
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.80.11.3168
Subject(s) - missense mutation , precocious puberty , luteinizing hormone , endocrinology , medicine , mutation , genetics , biology , hormone , gene
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