MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis
Abstract
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 mutations in CPP. The search was conducted in seven electronic databases (Cochrane, EMBASE, LILACS, LIVIVO, PubMed, Scopus, and Web of Science) for...
Paper Details
Title
MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis
Published Date
Mar 25, 2019
Volume
3
Issue
5
Pages
979 - 995
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