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Combined effects of two mutations in von Willebrand disease 2M phenotype
ESSENTIALS: Compound heterozygosity causes a VWD2M phenotype in a child with severe bleeding symptoms. p.P1648fs*45 changes the folding of A2 domain altering VWF binding to GPIbα and type VI collagen. p.P1648fs*45 was considered as an apparent de novo mutation; AS‐PCR revealed paternal mosaicism. Bl...
Autores principales: | Woods, Adriana I., Paiva, Juvenal, Kempfer, Ana C., Primrose, Debora M., Blanco, Alicia N., Sanchez‐Luceros, Analía, Lazzari, María A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868045/ https://www.ncbi.nlm.nih.gov/pubmed/30046717 http://dx.doi.org/10.1002/rth2.12067 |
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