Thromb Haemost 1995; 73(05): 895
DOI: 10.1055/s-0038-1653890
Letters to the Editor
Schattauer GmbH Stuttgart

Molecular Analysis in Factor XIIIA Deficiency

S Aslam
Molecular Haematology Unit, Department of Haematology, Bristol Royal Infirmary, Bristol, UK
,
G R Standen
Molecular Haematology Unit, Department of Haematology, Bristol Royal Infirmary, Bristol, UK
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received12. Dezember 1994

Accepted after resubmission 08. Februar 1995

Publikationsdatum:
09. Juli 2018 (online)

 
  • 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