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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Ann Lab Med
Egile Nagusiak: Kim, Hee-Jung, Kim, Soon Ki, Yoo, Ki-Young, Lee, Ki-O, Yun, Jae Won, Kim, Sun-Hee, Kim, Hee-Jin, Park, Sang Kyu
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: The Korean Society for Laboratory Medicine 2019
Gaiak:
Original Article
Sarrera elektronikoa: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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