Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice-Reference-Cited by-同舟云学术

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice

Published:2022-01 Issue:1 Volume:109 Page:157-171
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Tan Chen,Meng Lanlan,Lv Mingrong,He Xiaojin,Sha Yanwei,Tang Dongdong,Tan Yaqi,Hu Tongyao,He Wenbin,Tu Chaofeng,Nie Hongchuan,Zhang Huan,Du Juan,Lu Guangxiu,Fan Li-qing,Cao Yunxia,Lin Ge,Tan Yue-Qiu

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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