Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes)

Journal of Thrombosis and Thrombolysis

Volumn 32, Issue 4, 2011, Pages 474-477

  Antonio, Girolami ^a   Silvia, Vettore ^a   Emanuela, Bonamigo ^a   Fabrizio, Fabris ^a  

^a UNIVERSITY OF PADUA MEDICAL SCHOOL   (Italy)

Author keywords

Macrothrombocytopenias; MYH9 gene; Thrombosis

Indexed keywords

ADULT; AGE; AGED; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; FECHTNER SYNDROME; FEMALE; GENETIC ASSOCIATION; HUMAN; MALE; MAY HEGGLIN ANOMALY; MUTATOR GENE; MYH9 GENE; NEPHROTIC SYNDROME; PRIORITY JOURNAL; RISK FACTOR; SEBASTIAN SYNDROME; THROMBOCYTOPENIA; THROMBOSIS;

CEREBRAL INFARCTION; HEARING LOSS, SENSORINEURAL; HUMANS; MOLECULAR MOTOR PROTEINS; MYOSIN HEAVY CHAINS; NEPHRITIS, HEREDITARY; THROMBOCYTOPENIA; THROMBOSIS;

EID: 82955248033     PISSN: 09295305     EISSN: 1573742X     Source Type: Journal    
DOI: 10.1007/s11239-011-0623-4     Document Type: Article

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