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Homozygous mutation in DNAAF4 causes primary ciliary dyskinesia in a Chinese family.
Jiang, Guoliang; Zou, Lijun; Long, Lingzhi; He, Yijun; Lv, Xin; Han, Yuanyuan; Yao, Tingting; Zhang, Yan; Jiang, Mao; Peng, Zhangzhe; Tao, Lijian; Xie, Wei; Meng, Jie.
Afiliação
  • Jiang G; Department of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Zou L; Hunan Key Laboratory of Organ Fibrosis, Central South University, Changsha, China.
  • Long L; Department of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
  • He Y; Hunan Key Laboratory of Organ Fibrosis, Central South University, Changsha, China.
  • Lv X; Department of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Han Y; Hunan Key Laboratory of Organ Fibrosis, Central South University, Changsha, China.
  • Yao T; Department of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Zhang Y; Hunan Key Laboratory of Organ Fibrosis, Central South University, Changsha, China.
  • Jiang M; Hunan Key Laboratory of Organ Fibrosis, Central South University, Changsha, China.
  • Peng Z; Department of Nephrology, Xiangya Hospital, Central South University, Changsha, China.
  • Tao L; Hunan Key Laboratory of Organ Fibrosis, Central South University, Changsha, China.
  • Xie W; Department of Nephrology, Xiangya Hospital, Central South University, Changsha, China.
  • Meng J; Department of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Front Genet ; 13: 1087818, 2022.
Article em En | MEDLINE | ID: mdl-36583018
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China