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Thromb Haemost 1995; 73(05): 895
DOI: 10.1055/s-0038-1653890
DOI: 10.1055/s-0038-1653890
Letters to the Editor
Molecular Analysis in Factor XIIIA Deficiency
Further Information
Publication History
Received12 December 1994
Accepted after resubmission 08 February 1995
Publication Date:
09 July 2018 (online)
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References
- 1 Kamura T, Okamura T, Murakawa M, Tsuda H, Teshima T, Shibuya T, Harada M, Niho Y. Deficiency of coagulation factor XIIIAsubunit caused by the dinucleotide deletion at the 5’ end of exon III. J Clin Invest 1992; 90: 315-319
- 2 Board P, Coggan M, Miloszewski K. Identification of a point mutation in factor XIIIAsubunit deficiency. Blood 1992; 80: 937-941
- 3 Standen GR, Bowen DJ. Factor XIIIABristol 1: detection of a nonsense mutation (Arg171→stop codon) in factor XIIIAsubunit deficiency. Brit J Haematol 1993; 85: 769-772
- 4 Mikkola H, Syrjala M, Rasi V, Vahtera E, Hamalainen E, Peltonen L, Palotie A. Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levels. Blood 1994; 84: 517-525