[A homozygous variant in a consanguineous pedigree with inherited protein S deficiency].

Xie, H X; Jin, Y H; Yang, L L; Xie, Y Y; Liu, S Q; Luo, S S; Wang, M S

Xie, H X; Jin, Y H; Yang, L L; Xie, Y Y; Liu, S Q; Luo, S S; Wang, M S.

Afiliação

Xie HX; Center of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325015, China.
Jin YH; Center of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325015, China.
Yang LL; Center of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325015, China.
Xie YY; Center of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325015, China.
Liu SQ; Center of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325015, China.
Luo SS; Center of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325015, China.
Wang MS; Center of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325015, China.

Zhonghua Jie He He Hu Xi Za Zhi ; 44(4): 360-364, 2021 Apr 12.

Article em Zh | MEDLINE | ID: mdl-33832024

Assuntos

Deficiência de Proteína S; Consanguinidade; Éxons; Família; Humanos; Masculino; Mutação; Linhagem; Deficiência de Proteína S/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência de Proteína S Limite: Humans / Male Idioma: Zh Revista: Zhonghua Jie He He Hu Xi Za Zhi Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

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