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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Published in: | Blood Vol. 127; no. 23; pp. 2781 - 2782 |
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Main Authors: | , |
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 |
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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 |