Characterization of a large deletion that leads to congenital factor XIII deficiency

Rinsho byori. The Japanese journal of clinical pathology

Volumn 56, Issue 3, 2008, Pages 187-194

  Otaki, Manabu ^a   Inaba, Hiroshi ^a   Shinozawa, Keiko ^a   Fujita, Susumu ^a   Amano, Kagehiro ^a   Fukutake, Katsuyuki ^a  

^a TOKYO MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGEN; BLOOD CLOTTING FACTOR 13;

ARTICLE; BLOOD CLOTTING FACTOR 13 DEFICIENCY; CASE REPORT; EXON; FRAMESHIFT MUTATION; GENE DELETION; GENETICS; HUMAN; IMMUNOLOGY; MALE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANTIGENS; EXONS; FACTOR XIII; FACTOR XIII DEFICIENCY; FRAMESHIFT MUTATION; HUMANS; MALE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE DELETION;

EID: 43349092502     PISSN: 00471860     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)