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

BACKGROUND: von Willebrand disease (VWD), characterized by quantitative or qualitative defects of von Willebrand factor (VWF), is the most common inheritable bleeding disorder. Data regarding the genetic background of VWD in Korean patients is limited. To our knowledge, this is the first comprehensi...

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Detalhes bibliográficos
Publicado no:Ann Lab Med
Main Authors: Kim, Hee-Jung, Kim, Soon Ki, Yoo, Ki-Young, Lee, Ki-O, Yun, Jae Won, Kim, Sun-Hee, Kim, Hee-Jin, Park, Sang Kyu
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Society for Laboratory Medicine 2019
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6660331/
https://ncbi.nlm.nih.gov/pubmed/31240882
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3343/alm.2019.39.6.545
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