They're not your daddy's inherited platelet disorders anymore

Journal of Thrombosis and Haemostasis

Volumn 11, Issue 11, 2013, Pages 2037-2038

  Lambert, M P ^a,b   Poncz, M ^a,b  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLI1 PROTEIN; GFI1B PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX1; UNCLASSIFIED DRUG; GFI1B PROTEIN, HUMAN; ONCOPROTEIN; REPRESSOR PROTEIN;

BERNARD SOULIER DISEASE; CHROMOSOME 9; FRAMESHIFT MUTATION; GLANZMANN DISEASE; HUMAN; MEGAKARYOPOIESIS; NONHUMAN; NOTE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; THROMBOCYTE ANOMALY; THROMBOCYTE DISORDER; THROMBOCYTE STRUCTURE; THROMBOCYTOPENIA; VON WILLEBRAND DISEASE; WISKOTT ALDRICH SYNDROME; ZINC FINGER MOTIF; FEMALE; GENETICS; MALE; MUTATION; PATHOLOGY; THROMBOCYTE;

BLOOD PLATELET DISORDERS; BLOOD PLATELETS; FEMALE; HUMANS; MALE; MUTATION; PROTO-ONCOGENE PROTEINS; REPRESSOR PROTEINS;

EID: 84887536982     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/jth.12405     Document Type: Note

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