Haemophilia B mutations in Sweden: a population-based study of mutational heterogeneity-Reference-Cited by-同舟云学术

Haemophilia B mutations in Sweden: a population-based study of mutational heterogeneity

Published:2001-04 Issue:1 Volume:113 Page:81-86
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Ljung Rolf,Petrini Pia,Tengborn Lilian,Sjörin Elsy

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.02759.x/fullpdf

Reference36 articles.

1. Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations;Attali;Thrombosis and Haemostasis,1999

2. Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies;Becker;American Journal of Human Genetics,1996

3. A new MspI restriction fragment length polymorphism in the hemophilia B locus;Camerino;Human Genetics,1985

4. CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series;Chen;Human Genetics,1991

5. The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions;Cooper;Human Genetics,1990

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