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Platelet disorders: the next generation is in

In this issue of Blood, Simeoni et al describe exciting results using a high-throughput sequencing (HTS) platform with 63 targeted genes in patients with heritable bleeding and thrombotic disorders, and Stritt et al advance a diaphanous-related formin 1 (DIAPH1) variant as a cause of inherited macro...

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Detalles Bibliográficos
Publicado en:Blood
Autores principales: Rao, A. Koneti, Songdej, Natthapol
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society of Hematology 2016
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4900952/
https://ncbi.nlm.nih.gov/pubmed/27282940
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2016-04-703215
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