Deficiency of coagulation factor XIII A subunit caused by the dinucleotide deletion at the 5' end of exon III - Kamura, T; Okamura, T; Murakawa, M; Tsuda, H; Teshima, T; Shibuya, T; Harada, M; Niho, Y (The Journal of clinical investigation, 1992)
Keywords: Alleles; Base Sequence; Biological and medical sciences; cDNA; coagulation factor XIII; deficiency; deletion; exons; Factor XIII - genetics; Factor XIII Deficiency - genetics; Gene Expression; Genes; Hematologic and hematopoietic diseases; Humans; Male; man; Medical sciences; Middle Aged; Molecular Sequence Data; Mutation; nucleotide sequence; Oligodeoxyribonucleotides - chemistry; Pedigree; Polymerase Chain Reaction; RNA, Messenger - genetics; Human; Molecular form; Nucleotide sequence; Deficiency; Factor XIII; Hemopathy; Case study; Exon; Gene; Deletion; Molecular biology; Coagulation factor; Coagulopathy