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.
Original language | English (US) |
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Pages (from-to) | 2781-2782 |
Number of pages | 2 |
Journal | Blood |
Volume | 127 |
Issue number | 23 |
DOIs |
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State | Published - Jun 9 2016 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Immunology
- Hematology
- Cell Biology