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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Dettagli Bibliografici
Pubblicato in:J Endocr Soc
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Endocrine Society 2019
Soggetti:
Meta-Analysis
Accesso online: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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