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Am J Hum Genet:Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratospermia in Humans and Mice

发布时间:2020-08-15 浏览次数:10

Xiaojin He,Chunyu Liu,Xiaoyu Yang,Mingrong Lv,Xiaoqing Ni,Qiang Li,Huiru Cheng,Wangjie Liu,Shixiong Tian,Huan Wu,Yang Gao,Chenyu Yang,Qing Tan,Jiangshan Cong,Dongdong Tang,Jingjing Zhang,Bing Song,Yading Zhong,Hang Li,Weiwei Zhi,Xiaohong Mao,Feifei Fu,Lei Ge,Qunshan Shen,Manyu Zhang,Hexige Saiyin,Li Jin,Yuping Xu,Ping Zhou,Zhaolian Wei,Feng Zhang,Yunxia Cao. Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice[J]. The American Journal of Human Genetics,2020,107(3).

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Bi-allelicLoss-of-functionVariantsinCFAP58CauseFlagellarAxonemeandMitochondrialSheathDefectsandAsthenoteratospermiainHumansandMice.pdf