MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis

MKRN3 mutations represent the most common genetic cause of central precocious puberty (CPP) but associations between genotype and clinical features have not been extensively explored. This systematic review and meta-analysis investigated genotype-phenotype associations and prevalence of MKRN3 mutati...

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Detalles Bibliográficos
Autores principales: Valadares, Luciana Pinto, Meireles, Cinthia Gabriel, De Toledo, Isabela Porto, Santarem de Oliveira, Renata, Gonçalves de Castro, Luiz Cláudio, Abreu, Ana Paula, Carroll, Rona S, Latronico, Ana Claudia, Kaiser, Ursula B, Guerra, Eliete Neves Silva, Lofrano-Porto, Adriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Meta-Analysis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483926/
https://www.ncbi.nlm.nih.gov/pubmed/31041429
http://dx.doi.org/10.1210/js.2019-00041

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483926/
https://www.ncbi.nlm.nih.gov/pubmed/31041429
http://dx.doi.org/10.1210/js.2019-00041

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