Open AccessWhole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals newDNAH1mutations
Author(s) -
Amir AmiriYekta,
Charles Coutton,
ZineEddine Kherraf,
Thomas Karaouzène,
Pauline Le Tanno,
Mohammad Hossein Sanati,
Marjan Sabbaghian,
Navid Almadani,
Mohammad Ali Sadighi Gilani,
Seyedeh Hanieh Hosseini,
Salahadin Bahrami,
Abbas Daneshipour,
Maurizio Bini,
Christophe Arnoult,
Roberto Colombo,
Hamid Gourabi,
Pierre F. Ray
Publication year - 2016
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/dew262
Subject(s) - exome sequencing , biology , flagellum , genetics , sperm , exome , mutation , evolutionary biology , computational biology , gene
Can whole-exome sequencing (WES) of patients with multiple morphological abnormalities of the sperm flagella (MMAF) identify causal mutations in new genes or mutations in the previously identified dynein axonemal heavy chain 1 (DNAH1) gene?
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