Autosomal dominant macrothrombocytopenia caused by a rare GPIBB variant: The importance of DNA sequencing
Int J Lab Hematol
.
2020 Jun;42(3):e98-e100.
doi: 10.1111/ijlh.13136.
Epub 2019 Dec 2.
Authors
Pieter M De Kesel
1
,
Anna Vantilborgh
2
,
Jan Dierick
3
,
Ariane Luyckx
3
,
Sarah Debussche
4
,
Kathleen Freson
5
,
Katrien M J Devreese
1
Affiliations
1
Department of Laboratory Medicine, Ghent University Hospital, Ghent, Belgium.
2
Department of Hematology, Ghent University Hospital, Ghent, Belgium.
3
Department of Laboratory Medicine, AZ Maria Middelares, Ghent, Belgium.
4
Department of Hematology, AZ Maria Middelares, Ghent, Belgium.
5
Department of Cardiovascular Sciences, Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.
PMID:
31793234
DOI:
10.1111/ijlh.13136
No abstract available
Publication types
Letter
Comment
MeSH terms
Blood Platelet Disorders*
Humans
Sequence Analysis, DNA