A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty

✍ Scribed by Sandro Cocco; Antonella Meloni; Maria Giuseppina Marini; Antonio Cao; Paolo Moi

• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 229 KB
• Volume: 7
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/(sici)1098-1004(1996)7:2<164::aid-humu13>3.0.co;2-0

✦ Synopsis

Communicated trj F a d Chehab

Familial male-limited precocious puberty (FMPP) is an autosomal dominant condition that affects exclusively boys. The isosexual precocious