Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses-Reference-Cited by-同舟云学术

Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses

Published:2019-11-01 Issue:6 Volume:39 Page:545-551
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Kim Hee-Jung¹²^ORCID,Kim Soon Ki³^ORCID,Yoo Ki-Young⁴^ORCID,Lee Ki-O⁵^ORCID,Yun Jae Won¹^ORCID,Kim Sun-Hee¹^ORCID,Kim Hee-Jin¹^ORCID,Park Sang Kyu⁶^ORCID

Affiliation:

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

2. Department of Laboratory Medicine, CHA Gangnam Medical Center, CHA University School of Medicine, Seoul, Korea

3. Department of Pediatrics, College of Medicine, Inha University Hospital, Incheon, Korea

4. Korea Hemophilia Foundation, Seoul, Korea

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

6. Department of Pediatrics, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea

Funder

Korea Hemophilia Foundation

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

https://synapse.koreamed.org/pdf/10.3343/alm.2019.39.6.545

Reference31 articles.

1. Epidemiological investigation of the prevalence of von Willebrand's disease

2. The genetic basis of von Willebrand disease

3. Structure of the gene for human von Willebrand factor

4. Sequence and structure relationships within von Willebrand factor

5. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

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