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Mutations in inherited fibrinogen disorders correlated with clinical features in the Chinese population.
Wan, Yafang; Li, Tian; Zhang, Wei; Wang, Liying; Zhang, Yu; Liao, Pu; Liu, Shiqiang.
Afiliação
  • Wan Y; Department of Clinical Laboratory, Chongqing General Hospital, Chongqing, 400014, People's Republic of China.
  • Li T; Department of Clinical Laboratory, Chongqing General Hospital, Chongqing, 400014, People's Republic of China.
  • Zhang W; Department of Clinical Laboratory, The Fourth People's Hospital of Chongqing, Chongqing, 400014, People's Republic of China.
  • Wang L; Department of Clinical Laboratory, Chongqing General Hospital, Chongqing, 400014, People's Republic of China.
  • Zhang Y; Department of Clinical Laboratory, Chongqing General Hospital, Chongqing, 400014, People's Republic of China.
  • Liao P; Department of Clinical Laboratory, Chongqing General Hospital, Chongqing, 400014, People's Republic of China. liaopu@sina.com.
  • Liu S; Department of Cardiothoracic Surgery, Nanchong Central Hospital, Nanchong, 637900, Sichuan, People's Republic of China. liushiqiangls1979@163.com.
J Thromb Thrombolysis ; 51(4): 1127-1131, 2021 May.
Article em En | MEDLINE | ID: mdl-32939696
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrinogênio / Afibrinogenemia Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En 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: Fibrinogênio / Afibrinogenemia Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article