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[A family with hereditary FⅪ deficiency caused by compound heterozygous mutation].
Zheng, X Y; Jin, Y H; Xu, Y Y; Yang, L L; Zhu, L Q; Wang, H H; Jiang, S T; Wang, M S.
Afiliação
  • Zheng XY; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Jin YH; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Xu YY; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Yang LL; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Zhu LQ; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Wang HH; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Jiang ST; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Wang MS; The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
Zhonghua Xue Ye Xue Za Zhi ; 42(8): 687-689, 2021 08 14.
Article em Zh | MEDLINE | ID: mdl-34547878
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação Limite: Humans Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação Limite: Humans Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article