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 inBlood Vol. 127; no. 23; pp. 2781 - 2782
Main Authors Rao, A.Koneti, Songdej, Natthapol
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 09.06.2016
American Society of Hematology
SeriesPlatelets and Thrombopoiesis
Subjects
Blood Platelet Disorders
Blood Platelets
High-Throughput Nucleotide Sequencing
Humans
Inside
Platelet Aggregation
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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