Platelet disorders: The next generation is in

A. Koneti Rao, Natthapol Songdej

Research output: Contribution to journalComment/debatepeer-review

2 Scopus citations

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 languageEnglish (US)
Pages (from-to)2781-2782
Number of pages2
JournalBlood
Volume127
Issue number23
DOIs
StatePublished - Jun 9 2016

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

Fingerprint Dive into the research topics of 'Platelet disorders: The next generation is in'. Together they form a unique fingerprint.

Cite this