Literature DB >> 33423959

Novel compound heterozygous variants in dynein axonemal heavy chain 17 cause asthenoteratospermia with sperm flagellar defects.

Bing Song1, Chunyu Liu2, Yang Gao1, Jordan Lee Marley3, Weiyu Li2, Xiaoqin Ni1, Wangjie Liu2, Yujie Chen1, Jiajia Wang1, Chao Wang1, Ping Zhou1, Zhaolian Wei1, Xiaojin He4, Feng Zhang5, Yunxia Cao6.   

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Year:  2020        PMID： 33423959     DOI： 10.1016/j.jgg.2020.07.004

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN： 1673-8527            Impact factor:   4.275


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  2 in total

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

Authors:  Chen Tan; Lanlan Meng; Mingrong Lv; Xiaojin He; Yanwei Sha; Dongdong Tang; Yaqi Tan; Tongyao Hu; Wenbin He; Chaofeng Tu; Hongchuan Nie; Huan Zhang; Juan Du; Guangxiu Lu; Li-Qing Fan; Yunxia Cao; Ge Lin; Yue-Qiu Tan
Journal:  Am J Hum Genet       Date:  2021-12-20       Impact factor: 11.043

2.  Identification of DNAH17 Variants in Han-Chinese Patients With Left-Right Asymmetry Disorders.

Authors:  Xuehui Yu; Lamei Yuan; Sheng Deng; Hong Xia; Xiaolong Tu; Xiong Deng; Xiangjun Huang; Xiao Cao; Hao Deng
Journal:  Front Genet       Date:  2022-05-27       Impact factor: 4.772
  2 in total

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