Novel IFT140 variants cause spermatogenic dysfunction in humans

Novel IFT140 variants cause spermatogenic dysfunction in humans

Abstract Background The intraflagellar transport protein 140 homolog (IFT140) is involved in the process of intraflagellar transport (IFT), a process that is essential for the formation and maintenance of most eukaryotic cilia and flagella. Variants IFT140 have been reported to account for ciliopath...

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Bibliographic Details
Main Authors: Xiong Wang, Yan‐wei Sha, Wen‐ting Wang, Yuan‐qing Cui, Jie Chen, Wei Yan, Xiao‐tao Hou, Li‐bin Mei, Cui‐cui Yu, Jiahui Wang
Format: Article
Language:English
Published: Wiley 2019-09-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
genetic variation
IFT140
intraflagellar transport
male infertility
spermatogenic dysfunction
Online Access:https://doi.org/10.1002/mgg3.920

Internet

https://doi.org/10.1002/mgg3.920

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