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Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.
Xu, Qiyu; Wang, Mingshan; Jin, Yanhui; Liu, Siqi; Luo, Shasha; Yang, Lihong.
Affiliation
  • Xu Q; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Blood Coagul Fibrinolysis ; 32(8): 596-602, 2021 Dec 01.
Article in En | MEDLINE | ID: mdl-34261859
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein C / Protein C Deficiency Type of study: Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2021 Document type: Article Affiliation country: China Country of publication: United kingdom
Fulltext
Add to My VHL
Print
XML
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein C / Protein C Deficiency Type of study: Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 2021 Document type: Article Affiliation country: China Country of publication: United kingdom