A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family-Reference-Cited by-同舟云学术

A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family

Published:2017-04-11 Issue:5 Volume:34 Page:683-694
ISSN:1058-0468
Container-title:Journal of Assisted Reproduction and Genetics
language:en
Short-container-title:J Assist Reprod Genet

Author:

Okutman Ozlem,Muller Jean,Skory Valerie,Garnier Jean Marie,Gaucherot Angeline,Baert Yoni,Lamour Valérie,Serdarogullari Munevver,Gultomruk Meral,Röpke Albrecht,Kliesch Sabine,Herbepin Viviana,Aknin Isabelle,Benkhalifa Moncef,Teletin Marius,Bakircioglu Emre,Goossens Ellen,Charlet-Berguerand Nicolas,Bahceci Mustafa,Tüttelmann Frank,Viville STéphane

Funder

Agence Nationale de la Recherche

Fondation Maladies Rares

Agence de la Biomédecine

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Developmental Biology,Obstetrics and Gynaecology,Genetics,Reproductive Medicine,General Medicine

Link

http://link.springer.com/article/10.1007/s10815-017-0900-z/fulltext.html

Reference59 articles.

1. Krausz C, Giachini C, Lo Giacco D, Daguin F, Chianese C, Ars E, Ruiz-Castane E, Forti G, Rossi E. High resolution X chromosome-specific array-CGH detects new CNVs in infertile males. PLoS One. 2012;7:e44887.