A Novel Homozygous Missense <b><i>FSHR</i></b> Variant Associated with Hypergonadotropic Hypogonadism in Two Siblings from a Brazilian Family-Reference-Cited by-同舟云学术

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A Novel Homozygous Missense FSHR Variant Associated with Hypergonadotropic Hypogonadism in Two Siblings from a Brazilian Family

Published:2017 Issue:3 Volume:11 Page:137-142
ISSN:1661-5425
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

França Monica M.,Lerario Antonio M.,Funari Mariana F.A.,Nishi Mirian Y.,Narcizo Amanda M.,de Mello Maricilda P.,Guerra-Junior Gil,Maciel-Guerra Andrea T.,Mendonça Berenice B.

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Restoring function to inactivating G protein‐coupled receptor variants in the hypothalamic–pituitary–gonadal axis¹;Journal of Neuroendocrinology;2024-06-09

2. Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing;BMC Medical Genomics;2024-04-22

3. The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea;Annals of Pediatric Endocrinology & Metabolism;2023-03-31

4. Identification and characterization of novel compound heterozygous variants in FSHR causing primary ovarian insufficiency with resistant ovary syndrome;Frontiers in Endocrinology;2023-01-10

5. Disorders of the Ovary;Endocrinology;2023

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