Cargando…
Mutation spectrum and genotype-phenotype correlations in a large French cohort of MYH9-Related Disorders
MYH9-Related Disorders are a group of rare autosomal dominant platelet disorders presenting as nonsyndromic forms characterized by macrothrombocytopenia with giant platelets and leukocyte inclusion bodies or as syndromic forms combining these hematological features with deafness and/or nephropathy a...
Autores principales: | Saposnik, Béatrice, Binard, Sylvie, Fenneteau, Odile, Nurden, Alan, Nurden, Paquita, Hurtaud-Roux, Marie-Françoise, Schlegel, Nicole |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113270/ https://www.ncbi.nlm.nih.gov/pubmed/25077172 http://dx.doi.org/10.1002/mgg3.68 |
Ejemplares similares
-
Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy
por: Nurden, Paquita, et al.
Publicado: (2020) -
Inherited thrombocytopenias: history, advances and perspectives
por: Nurden, Alan T., et al.
Publicado: (2020) -
Deep Vein Thrombosis, Raynaud's Phenomenon, and Prinzmetal Angina in a Patient with Glanzmann Thrombasthenia
por: Nurden, Alan, et al.
Publicado: (2012) -
The Nbeal2(−/−) mouse as a model for the gray platelet syndrome
por: Deppermann, Carsten, et al.
Publicado: (2013) -
Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders
por: Latger-Cannard, Veronique, et al.
Publicado: (2016)