Platelet disorders: The next generation is in

A. Koneti Rao, Natthapol Songdej

Research output: Contribution to journal › Comment/debate

2 Citations (Scopus)

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 loss 1,2 .

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

Fingerprint

Audition
Platelets
Hearing Loss
Blood
Blood Platelets
Genes
Throughput
Hemorrhage
formin 1

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

Cite this

Koneti Rao, A. ; Songdej, Natthapol. / Platelet disorders : The next generation is in. In: Blood. 2016 ; Vol. 127, No. 23. pp. 2781-2782.
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Koneti Rao, A & Songdej, N 2016, 'Platelet disorders: The next generation is in', Blood, vol. 127, no. 23, pp. 2781-2782. https://doi.org/10.1182/blood-2016-04-703215

Platelet disorders : The next generation is in. / Koneti Rao, A.; Songdej, Natthapol.

In: Blood, Vol. 127, No. 23, 09.06.2016, p. 2781-2782.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Platelet disorders

T2 - The next generation is in

AU - Koneti Rao, A.

AU - Songdej, Natthapol

PY - 2016/6/9

Y1 - 2016/6/9

N2 - 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 .

AB - 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 .

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DO - 10.1182/blood-2016-04-703215

M3 - Comment/debate

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AN - SCOPUS:84974605238

VL - 127

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Koneti Rao A, Songdej N. Platelet disorders: The next generation is in. Blood. 2016 Jun 9;127(23):2781-2782. https://doi.org/10.1182/blood-2016-04-703215

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