Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty.

Genomic DNA from 32 unrelated families with male-limited precocious puberty was examined for the previously described Asp-578-->Gly, Met-571-->Ile, and Thr-577-->Ile mutations in transmembrane helix 6 of the human luteinizing hormone receptor (hLHR). Twenty-eight families had the inherited...

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Detalhes bibliográficos
Main Authors: Laue, L, Chan, W Y, Hsueh, A J, Kudo, M, Hsu, S Y, Wu, S M, Blomberg, L, Cutler, G B
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC42391/
https://ncbi.nlm.nih.gov/pubmed/7892197
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