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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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Laboratory Medicine 2019
Materias:
Original Article
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

Internet

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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