Platelet disorders: The next generation is in

A. Koneti Rao; Natthapol Songdej

doi:10.1182/blood-2016-04-703215

Platelet disorders: The next generation is in

A. Koneti Rao
, Natthapol Songdej

Research output: Contribution to journal › Comment/debate › peer-review

4 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 loss^1,2.

Original language	English (US)
Pages (from-to)	2781-2782
Number of pages	2
Journal	Blood
Volume	127
Issue number	23
DOIs	https://doi.org/10.1182/blood-2016-04-703215
State	Published - Jun 9 2016

All Science Journal Classification (ASJC) codes

Biochemistry
Immunology
Hematology
Cell Biology

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10.1182/blood-2016-04-703215

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title = "Platelet disorders: The next generation is in",

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.",

author = "\{Koneti Rao\}, A. and Natthapol Songdej",

note = "Publisher Copyright: {\textcopyright} 2016 by The American Society of Hematology.",

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doi = "10.1182/blood-2016-04-703215",

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AU - Koneti Rao, A.

AU - Songdej, Natthapol

PY - 2016/6/9

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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 loss1,2.

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 loss1,2.

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UR - https://www.scopus.com/pages/publications/84974605238#tab=citedBy

U2 - 10.1182/blood-2016-04-703215

DO - 10.1182/blood-2016-04-703215

M3 - Comment/debate

C2 - 27282940

AN - SCOPUS:84974605238

SN - 0006-4971

VL - 127

SP - 2781

EP - 2782

JO - Blood

JF - Blood

IS - 23

ER -

Platelet disorders: The next generation is in

Abstract

All Science Journal Classification (ASJC) codes

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