Correlation between different FGFR1 mutations and congenital hypogonadotropic hypogonadism

Objective To investigate whether multiple gene mutations were existed to cause congenital hypogonadotropic hypogonadism(CHH), by screening genes in CHH patients with FGFR1 mutations. Methods FGFR1 mutations were identified in 15 CHH patients. Other CHH-related genes were screened in these patients...

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Bibliografiske detaljer

Hovedforfatter:	YANG Yufan, WANG Xi, NIE Min, WU Xueyan, MAO Jiangfeng
Format:	Artigo
Sprog:	Chinês
Udgivet:	Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College. 2023-05-01
Serier:	Jichu yixue yu linchuang
Fag:	congenital hypogonadotropic hypogonadism(chh)|fibroblast growth factor receptor 1(fgfr1)|digenic mutation
Online adgang:	http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2023-43-5-733.pdf
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