Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients

Journal of Thrombosis and Haemostasis

Volumn 3, Issue 3, 2005, Pages 482-488

  Nair, S ^a   Ghosh, K ^a   Shetty, S ^a   Mohanty, Dipika ^a  

^a KEM HOSPITAL   (India)

Author keywords

Glanzmann thrombasthenia; Mutations

Indexed keywords

FIBRINOGEN RECEPTOR; GLYCOPROTEIN IIIA; BETA3 INTEGRIN;

ARTICLE; BLOOD CELL COUNT; CLINICAL ARTICLE; CONTROLLED STUDY; DENATURING GRADIENT GEL ELECTROPHORESIS; EXON; FEMALE; FLOW CYTOMETRY; GENE DELETION; GENE EXPRESSION REGULATION; GENETIC COUNSELING; GLANZMANN DISEASE; HUMAN; INDIA; MALE; MUTATIONAL ANALYSIS; POINT MUTATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; THROMBOCYTE AGGREGATION; WESTERN BLOTTING; GENETICS; MUTATION; NUCLEOTIDE SEQUENCE;

DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HUMANS; INDIA; INTEGRIN BETA3; MALE; MUTAGENESIS, INSERTIONAL; MUTATION; POINT MUTATION; SEQUENCE DELETION; THROMBASTHENIA;

EID: 23944442844     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2005.01159.x     Document Type: Article

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