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 mac...

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Bibliographic Details
Published in:Blood Vol. 127; no. 23; pp. 2781 - 2782
Main Authors: Rao, A.Koneti, Songdej, Natthapol
Format: Journal Article
Language:English
Published: United States Elsevier Inc 09-06-2016
American Society of Hematology
Series:Platelets and Thrombopoiesis
Subjects:
Online Access:Get full text
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Summary: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
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Commentary-1
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2016-04-703215