Platelet disorders: the next generation is in #MMPMID27282940
Rao AK; Songdej N
Blood 2016[Jun]; 127 (23): 2781-2 PMID27282940show ga
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 loss.1,2