about
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defectsWhole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsUse of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders.Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors.Comparison of multiple electrode aggregometry with lumi-aggregometry for the diagnosis of patients with mild bleeding disorders.
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description
researcher ORCID ID = 0000-0003-1405-9719
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wetenschapper
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name
Sian Drake
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Sian Drake
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Sian Drake
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Sian Drake
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type
label
Sian Drake
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Sian Drake
@en
Sian Drake
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Sian Drake
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prefLabel
Sian Drake
@ast
Sian Drake
@en
Sian Drake
@es
Sian Drake
@nl
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P1153
56494397700
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P496
0000-0003-1405-9719