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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Vydáno v:J Endocr Soc
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Endocrine Society 2019
Témata:
Meta-Analysis
On-line přístup: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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