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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Bibliografiske detaljer
Udgivet i:J Endocr Soc
Main Authors: 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
Format: Artigo
Sprog:Inglês
Udgivet: Endocrine Society 2019
Fag:
Meta-Analysis
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6483926/
https://ncbi.nlm.nih.gov/pubmed/31041429
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-00041
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