A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family-Reference-Cited by-同舟云学术

A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family

Published:2018-04-05 Issue:6 Volume:33 Page:1034-1037
ISSN:0268-1161
Container-title:Human Reproduction
language:en
Short-container-title:

Author:

Ben Khelifa M¹,Ghieh F¹,Boudjenah R¹²,Hue C³,Fauvert D¹,Dard R¹²,Garchon H J³,Vialard F¹²

Affiliation:

1. EA7404-GIG, UFR des Sciences de la Santé Simone Veil, UVSQ, 2 av de la source de la Bièvre, 78180 Montigny le Bretonneux, France

2. Genetics Laboratory, CHI de Poissy St Germain en Laye, 10 rue du champ gaillard, 78300 Poissy, France

3. UMR1179, Ufr des sciences de la Santé Simone Veil, UVSQ, 2 av de la source de la Bièvre, 78180, Montigny le Bretonneux, France

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine

Link

http://academic.oup.com/humrep/article-pdf/33/6/1034/24855452/dey073.pdf

Reference25 articles.

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2. Mutation in TDRD9 causes non-obstructive azoospermia in infertile men;Arafat;J Med Genet,2017

3. Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia;Ayhan;J Med Genet,2014

4. Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair;Bolcun-Filas;PLoS Genet,2009

5. Mutant cohesin in premature ovarian failure;Caburet;N Engl J Med,2014

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