A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in...
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
About this item
Full title
Author / Creator
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 and Viville, STéphane
Publisher
New York: Springer US
Journal title
Language
English
Formats
Publication information
Publisher
New York: Springer US
Subjects
More information
Scope and Contents
Contents
Purpose
The purpose of this study was to identify mutations that cause non-syndromic male infertility using whole exome sequencing of family cases.
Methods
We recruited a consanguineous Turkish family comprising nine siblings with male triplets; two of the triplets were infertile as well as one younger infertile brother. Whole exome sequen...
Alternative Titles
Full title
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
Authors, Artists and Contributors
Author / Creator
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
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5427651
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5427651
Other Identifiers
ISSN
1058-0468
E-ISSN
1573-7330
DOI
10.1007/s10815-017-0900-z
