Identification of a homozygous GFPT2 variant in a family with asthenozoospermia

Author:

Askari Masomeh,Kordi-Tamandani Dor Mohammad,Almadani Navid,McElreavey Kenneth,Totonchi Mehdi

Funder

Iran National Science Foundation

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference44 articles.

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4. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations;Amiri-Yekta;Hum. Reprod.,2016

5. Human male infertility caused by mutations in the CATSPER1 channel protein;Avenarius;Am. J. Hum. Genet.,2009

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