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[Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in different families].
Xu, Q Y; Yang, L L; Xie, H X; Jin, Y H; Li, X L; Zhou, X X; Liu, M N; Wang, M S.
Affiliation
  • Xu QY; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Yang LL; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Xie HX; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Jin YH; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Li XL; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Zhou XX; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Liu MN; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
  • Wang MS; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.
Zhonghua Xue Ye Xue Za Zhi ; 43(1): 35-40, 2022 Jan 14.
Article in Zh | MEDLINE | ID: mdl-35231991
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein C Deficiency Type of study: Prognostic_studies Limits: Humans Language: Zh Journal: Zhonghua Xue Ye Xue Za Zhi Year: 2022 Document type: Article Affiliation country:
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein C Deficiency Type of study: Prognostic_studies Limits: Humans Language: Zh Journal: Zhonghua Xue Ye Xue Za Zhi Year: 2022 Document type: Article Affiliation country: