High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic

BACKGROUND/AIMS: Recently, loss-of-function mutations in the MKRN3 gene have been implicated in the etiology of familial central precocious puberty (CPP) in both sexes. We aimed to analyze the frequency of MKRN3 mutations in boys with CPP and to compare the clinical and hormonal features of boys wit...

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Detalhes bibliográficos
Publicado no:Neuroendocrinology
Main Authors: Bessa, Danielle S., Macedo, Delanie B., Brito, Vinicius N., França, Monica M., Montenegro, Luciana R., Cunha-Silva, Marina, Silveira, Leticia G., Hummel, Tiago, Bergadá, Ignacio, Braslavsky, Debora, Abreu, Ana Paula, Dauber, Andrew, Mendonca, Berenice B., Kaiser, Ursula B., Latronico, Ana Claudia
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5195904/
https://ncbi.nlm.nih.gov/pubmed/27225315
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000446963
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