Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: Five novel mutations detected

Haemophilia

Volumn 17, Issue 5, 2011, Pages

  Shanbhag, S ^a   Shetty, S ^a   Ghosh, K ^a  

^a NATIONAL INSTITUTE OF IMMUNOHAEMATOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; BLOOD CLOTTING FACTOR 13A; GENOMIC DNA;

ADOLESCENT; ADULT; BLEEDING; BLOOD CLOTTING FACTOR 13 DEFICIENCY; BLOOD SAMPLING; BLOOD TRANSFUSION; CHILD; CHROMOSOME 6; CLINICAL ARTICLE; CONSANGUINITY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; LETTER; MALE; MISSENSE MUTATION; NONSENSE MUTATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RNA SPLICING; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; FACTOR XIII; FEMALE; FRAMESHIFT MUTATION; HEMOPHILIA A; HUMANS; MALE; MUTATION, MISSENSE; POLYMERASE CHAIN REACTION; YOUNG ADULT;

EID: 80052025085     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2011.02590.x     Document Type: Letter

References (9)

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