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Loss-of-function mutation in TSGA10 causes acephalic spermatozoa phenotype in human.
Ye, Yuanyuan; Wei, Xiaoli; Sha, Yanwei; Li, Na; Yan, Xiaohong; Cheng, Ling; Qiao, Duanrui; Zhou, Weidong; Wu, Rongfeng; Liu, Qiaobin; Li, Youzhu.
Afiliação
  • Ye Y; Reproductive Medicine Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
  • Wei X; School of Pharmaceutical Sciences, Xiamen University, Xiamen, China.
  • Sha Y; Department of Reproductive Medicine, Xiamen Maternity and Child Care Hospital, Xiamen, China.
  • Li N; Intensive Care Unit, Fujian Medical University Xiamen Humanity Hospital, Xiamen, China.
  • Yan X; Reproductive Medicine Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
  • Cheng L; Reproductive Medicine Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
  • Qiao D; Department of Gynecology, Second Hospital of Jilin University, Changchun, China.
  • Zhou W; Reproductive Medicine Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
  • Wu R; Reproductive Medicine Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
  • Liu Q; Center for Reproductive Medicine, the 174th Hospital of People's Liberation Army, Xiamen, China.
  • Li Y; Reproductive Medicine Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Mol Genet Genomic Med ; 8(7): e1284, 2020 07.
Article em En | MEDLINE | ID: mdl-32410354
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espermatozoides / Proteínas do Citoesqueleto / Teratozoospermia / Mutação com Perda de Função Limite: Adult / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espermatozoides / Proteínas do Citoesqueleto / Teratozoospermia / Mutação com Perda de Função Limite: Adult / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China