SUN-725 Clinical and Genetic Features of Families with Maternally Inherited Central Precocious Puberty

Context: The clinical recognition of familial central precocious puberty (CPP) has significantly increased in the last years. This fact can be related to the recent descriptions of genetic causes associated with this pediatric condition, such as loss-of-function mutations of two imprinted genes (MKR...

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保存先:
書誌詳細
出版年:J Endocr Soc
主要な著者: Tinano, Flávia Rezende, Canton, Ana Pinheiro Machado, Montenegro, Luciana Ribeiro, Leal, Andrea de Castro, Ramos, Carolina, Piovesan, Maiara Ribeiro, Seraphim, Carlos Eduardo, de Faria, Aline Guimarães, Mendonca, Berenice Bilharinho, Brito, Vinicius Nahime, Latronico, Ana Claudia
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2020
主題:
Genetics and Development (including Gene Regulation)
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207300/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1315
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