Genetic Confirmation of Congenital Factor V Deficiency in Korean Patients-Reference-Cited by-同舟云学术

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Genetic Confirmation of Congenital Factor V Deficiency in Korean Patients

Published:2016-03-01 Issue:2 Volume:36 Page:182-184
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Park Chang-Hun¹,Yoo Kiyoung²,Lee Ki-O³,Kim Sun-Hee¹,Sung Ki-Woong⁴,Kim Hee-Jin¹

Affiliation:

1. Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

2. Korea Hemophilia Foundation, Seoul, Korea

3. Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Korea

4. Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

Funder

Korea Hemophilia Foundation

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

http://synapse.koreamed.org/pdf/10.3343/alm.2016.36.2.182

Reference10 articles.

1. Asp68His mutation in the A1 domain of human factor V causes impaired secretion and ineffective translocation

2. A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family

3. Parahemophilia: New Insights into Factor V Deficiency

Cited by 8 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. Congenital Factor V Deficiency from Compound Heterozygous Mutations with a Novel Variant c.5403del (p.Lys1801AsnfsTer11) in the F5 Gene: A Case Report;Laboratory Medicine Online;2024-04-01

2. Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813∗ and two variants specific to East Asians;Blood Coagulation & Fibrinolysis;2022-08-22

3. A novel mutation of congenital factor V deficiency in Henoch–Schönlein purpura;Pediatrics International;2020-08

4. Congenital factor V deficiency from compound heterozygous mutations with a novel variant c.2426del (p.Pro809Hisfs∗2) in the F5 gene;Medicine;2020-01

5. First description of the molecular and clinical characterization of hereditary factor V deficiency in Saudi Arabia;Blood Coagulation & Fibrinolysis;2019-07

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