Intron 1 factor VIII gene inversion in a population of Italian hemophilia A patients
Author:
Affiliation:
1. Correspondence: Federica Riccardi, Laboratory of Molecular Genetics and Diagnostic Biotechnology, Hospital of Parma, Via Gramsci, 14, 43100 Parma, Italy; e-mail:
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/100/9/3432/1259425/h82102003432a.pdf
Reference4 articles.
1. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe haemophilia A.;Bagnall;Blood.,2002
2. Two chimeric transcription units result from an inversion breaking intron 1 of the factor VIII gene and a region reportedly affected by reciprocal translocations in T-cell leukaemia.;Brinke;Hum Mol Gen.,1996
3. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.;Lakich;Nat Genet.,1993
4. Single-tube polymerase chain reaction for rapid diagnosis of the inversion hotspot of mutation in hemophilia A [letter].;Liu;Blood.,1998
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