Correlation between phenotype and genotype in a large unselected cohort of children with severe hemophilia A

Blood

Volumn 121, Issue 19, 2013, Pages 3946-3952

  Carcao, Manuel D ^a   Van Den Berg, H Marijke ^b   Ljung, Rolf ^c   Mancuso, Maria Elisa ^d  

^a UNIVERSITY OF TORONTO   (Canada)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c LUND UNIVERSITY   (Sweden)

^d FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILDHOOD DISEASE; COHORT ANALYSIS; CORRELATIONAL STUDY; DISEASE SEVERITY; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; GENOTYPE; HEMOPHILIA A; HUMAN; MAJOR CLINICAL STUDY; MULTICENTER STUDY; OUTCOME ASSESSMENT; PHENOTYPE; PRIORITY JOURNAL; PROPHYLAXIS; PROSPECTIVE STUDY; ADOLESCENT; ADULT; BLEEDING; CHILD; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETICS; PRESCHOOL CHILD; SAMPLE SIZE; SEVERITY OF ILLNESS INDEX; STOP CODON;

BLOOD CLOTTING FACTOR 8;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CODON, NONSENSE; COHORT STUDIES; FACTOR VIII; GENETIC ASSOCIATION STUDIES; GENETIC HETEROGENEITY; GENOTYPE; HEMOPHILIA A; HEMORRHAGE; HUMANS; PHENOTYPE; SAMPLE SIZE; SEVERITY OF ILLNESS INDEX; YOUNG ADULT;

MLCS; MLOWN;

EID: 84880473815     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2012-11-469403     Document Type: Article

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