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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...
Autores principales: | Kim, Hee-Jung, Kim, Soon Ki, Yoo, Ki-Young, Lee, Ki-O, Yun, Jae Won, Kim, Sun-Hee, Kim, Hee-Jin, Park, Sang Kyu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Laboratory Medicine
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6660331/ https://www.ncbi.nlm.nih.gov/pubmed/31240882 http://dx.doi.org/10.3343/alm.2019.39.6.545 |
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