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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...
Gorde:
| Argitaratua izan da: | Blood |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
American Society of Hematology
2016
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| Gaiak: | |
| Sarrera elektronikoa: | 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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