A Novel Missense Mutation Asp506Gly in Exon 13 of the F11 Gene in an Asymptomatic Korean Woman with Mild Factor XI Deficiency-Reference-Cited by-同舟云学术

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A Novel Missense Mutation Asp506Gly in Exon 13 of the F11 Gene in an Asymptomatic Korean Woman with Mild Factor XI Deficiency

Published:2011-10-01 Issue:4 Volume:31 Page:290-293
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Lee Jong Ho¹,Cho Hee Soon¹,Hyun Myung Soo²,Kim Hwa-Young³,Kim Hee-Jin⁴

Affiliation:

1. Departments of Laboratory Medicine, Yeungnam University College of Medicine, Daegu, Korea

2. Departments of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea

3. Departments of Biochemistry & Molecular Biology, Yeungnam University College of Medicine, Daegu, Korea

4. Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University College of Medicine, Seoul, Korea

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Link

https://synapse.koreamed.org/pdf/10.3343/kjlm.2011.31.4.290

Reference25 articles.

1. The coagulation cascade: initiation, maintenance, and regulation

2. Factor XI Activation in a Revised Model of Blood Coagulation

3. Association of factor XI and high molecular weight kininogen in human plasma.

4. Molecular Characterization of FXI Deficiency

5. Organization of the gene for human factor XI

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cys482Trp Missense Mutation in the Coagulation Factor XI Gene (F11) in a Korean Patient with Factor XI Deficiency;Annals of Laboratory Medicine;2014-07-01

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