A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing-Reference-Cited by-同舟云学术

A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing

Published:2016-02-23 Issue:4 Volume:31 Page:905-914
ISSN:0268-1161
Container-title:Human Reproduction
language:en
Short-container-title:Hum. Reprod.

Author:

Bramble Matthew S.,Goldstein Ellen H.,Lipson Allen,Ngun Tuck,Eskin Ascia,Gosschalk Jason E.,Roach Lara,Vashist Neerja,Barseghyan Hayk,Lee Eric,Arboleda Valerie A.,Vaiman Daniel,Yuksel Zafer,Fellous Marc,Vilain Eric

Funder

DSD Translational Research Network

Neuroendocrinology, Sex Differences and Reproduction

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine

Link

http://academic.oup.com/humrep/article-pdf/31/4/905/7052742/dew025.pdf

Reference51 articles.

1. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

2. Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene

3. Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability

4. A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics

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