Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease

The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other mild bleeding diatheses. We previously showed that mutations in the platelet P2Y(12) ADP receptor gene (P2RY12) could contribute to the bleeding phenotype in patients with type 1 von Willebrand diseas...

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Detalles Bibliográficos
Autores principales: Stockley, Jacqueline, Nisar, Shaista P., Leo, Vincenzo C., Sabi, Essa, Cunningham, Margaret R., Eikenboom, Jeroen C., Lethagen, Stefan, Schneppenheim, Reinhard, Goodeve, Anne C., Watson, Steve P., Mundell, Stuart J., Daly, Martina E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667889/
https://www.ncbi.nlm.nih.gov/pubmed/26630678
http://dx.doi.org/10.1371/journal.pone.0143913

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