The Nbeal2(−/−) mouse as a model for the gray platelet syndrome

The gray platelet syndrome (GPS) is a rare, autosomal-recessive platelet disorder characterized by thrombocytopenia, large platelets lacking α-granules, and variable bleeding. GPS has been linked to mutations in the neurobeachin-like 2 gene (NBEAL2). We have recently characterized Nbeal2-deficient m...

Descripción completa

Detalles Bibliográficos
Autores principales: Deppermann, Carsten, Nurden, Paquita, Nurden, Alan T, Nieswandt, Bernhard, Stegner, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Addendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915564/
https://www.ncbi.nlm.nih.gov/pubmed/25003009
http://dx.doi.org/10.4161/rdis.26561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915564/
https://www.ncbi.nlm.nih.gov/pubmed/25003009
http://dx.doi.org/10.4161/rdis.26561

Ejemplares similares