Abstract
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 macrothrombocytopenia (MTP) and hearing loss1,2.
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CITATION STYLE
APA
Koneti Rao, A., & Songdej, N. (2016, June 9). Platelet disorders: The next generation is in. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2016-04-703215
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