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Journal Articles Gene Year : 2019

Identification of a homozygous GFPT2 variant in a family with asthenozoospermia

Abstract

Asthenozoospermia (ASZ) is a condition characterized by reduced sperm motility in semen affecting approximately 19% of infertile men. Major risk factors, particularly gene mutations, still remain unknown. The main aim of the present study was to identify novel genes and mutations that may influence human sperm motility.
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pasteur-03521835 , version 1 (11-01-2022)

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Masomeh Askari, Dor Mohammad Kordi-Tamandani, Navid Almadani, Ken Mcelreavey, Mehdi Totonchi. Identification of a homozygous GFPT2 variant in a family with asthenozoospermia. Gene, 2019, 699, pp.16-23. ⟨10.1016/j.gene.2019.02.060⟩. ⟨pasteur-03521835⟩

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