[Genetic Analysis of A Case of Congenital Dysfibrinogenemia Caused by Arg16His Mutation in Exon 2 of FGA].

Zhang, Yong-Lu; Liu, Shu-Yuan; Zhang, Zhang-Lin; Tao, Xiao-Yan; Peng, Xiao-Xiao; Kong, Yun-Yuan

Zhang, Yong-Lu; Liu, Shu-Yuan; Zhang, Zhang-Lin; Tao, Xiao-Yan; Peng, Xiao-Xiao; Kong, Yun-Yuan.

Afiliação

Zhang YL; Department of Laboratoria Examination, The First Affiliated Hospitul of Nanchang University, Nanchang 330006, Jiangxi Province, China.
Liu SY; Department of Laboratoria Examination, The First Affiliated Hospitul of Nanchang University, Nanchang 330006, Jiangxi Province, China.
Zhang ZL; Department of Laboratoria Examination, The First Affiliated Hospitul of Nanchang University, Nanchang 330006, Jiangxi Province, China.
Tao XY; Department of Laboratoria Examination, The First Affiliated Hospitul of Nanchang University, Nanchang 330006, Jiangxi Province, China.
Peng XX; Department of Laboratoria Examination, The First Affiliated Hospitul of Nanchang University, Nanchang 330006, Jiangxi Province, China.
Kong YY; Department of Laboratoria Examination, The First Affiliated Hospitul of Nanchang University, Nanchang 330006, Jiangxi Province, China. E-mail:11622525@qq.com.

Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 25(5): 1514-1517, 2017 Oct.

Article em Zh | MEDLINE | ID: mdl-29070135

Assuntos

Afibrinogenemia/genética; Éxons; Fibrinogênio/genética; Mutação; Humanos; Linhagem

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrinogênio / Éxons / Afibrinogenemia / Mutação Limite: Humans Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Assunto da revista: HEMATOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China

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