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A Case of Male-Limited Precocious Puberty Caused by a Point Mutation in the Second Transmembrane Domain of the Luteinizing Hormone Choriogonadotropin Receptor Gene

✍ Scribed by Koichi Yano; Leonard D. Kohn; Motoyasu Saji; Naoki Kataoka; Akimasa Okuno; Gordon B. Cutler; Jr.


Book ID
115578276
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
165 KB
Volume
220
Category
Article
ISSN
0006-291X

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## Communicated trj F a d Chehab Familial male-limited precocious puberty (FMPP) is an autosomal dominant condition that affects exclusively boys. The isosexual precocious