[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

Xu, Q Y; Yang, L L; Xie, H X; Jin, Y H; Li, X L; Zhou, X X; Liu, M N; Wang, M S.

Afiliação

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 em Zh | MEDLINE | ID: mdl-35231991

Assuntos

Deficiência de Proteína C; Humanos; Mutação; Mutação de Sentido Incorreto; Linhagem; Fenótipo; Proteína C/genética; Deficiência de Proteína C/genética

Palavras-chave

Genetic mutation; PROC gene; Protein C deficiency; Venous thrombosis

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiência de Proteína C Tipo de estudo: Prognostic_studies Limite: Humans Idioma: Zh Revista: Zhonghua Xue Ye Xue Za Zhi Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

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