Open AccessWhole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella
Author(s) -
Guillaume Martinez,
ZineEddine Kherraf,
Raoudha Zouari,
Sélima Fourati Ben Mustapha,
Antoine Saut,
Karin PernetGallay,
Anne Bertrand,
Marie Bidart,
Jean Pascal Hograindleur,
Amir AmiriYekta,
Mahmoud Kharouf,
Thomas Karaouzène,
Nicolas ThierryMieg,
Denis Dacheux,
Véronique Satre,
Mélanie Bonhivers,
Aminata Touré,
Christophe Arnoult,
Pierre F. Ray,
Charles Coutton
Publication year - 2018
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/dey264
Subject(s) - sanger sequencing , biology , sperm , exome sequencing , genetics , flagellum , gene , compound heterozygosity , mutation
Can whole-exome sequencing (WES) of infertile patients identify new genes responsible for multiple morphological abnormalities of the sperm flagella (MMAF)?
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