[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.

Afiliación

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 en Zh | MEDLINE | ID: mdl-29070135

Asunto(s)

Afibrinogenemia/genética; Exones; Fibrinógeno/genética; Mutación; Humanos; Linaje

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrinógeno / Exones / Afibrinogenemia / Mutación Límite: Humans Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: China

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