ArticleNucleic acids research1994
Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994.
Article in Nucleic acids research, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
10 citing papers in PubMed.
- Application of multigene panel testing for bleeding, thrombotic, and platelet disorders in patients and the general population in China.Molecular biomedicine · 2025Article
- Article
- Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).Journal of medical genetics · 1997Article
- gamma-Carboxyglutamic acids 36 and 40 do not contribute to human factor IX function.Protein science : a publication of the Protein Society · 1997Article
- The EMBL Nucleotide Sequence Database.Nucleic acids research · 1997Article
- A two-step recognition of signal sequences determines the translocation efficiency of proteins.The EMBO journal · 1996Article
- Haemophilia B (sixth edition): a database of point mutations and short additions and deletions.Nucleic acids research · 1996Article
- The European Bioinformatics Institute (EBI) databases.Nucleic acids research · 1996Article
- A general database for DNA sequence changes induced by mutagenesis of several bacterial and mammalian genes.Nucleic acids research · 1996Article
- X-ray structure of clotting factor IXa: active site and module structure related to Xase activity and hemophilia B.Proceedings of the National Academy of Sciences of the United States of America · 1995Article
Corrections and comments
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The fifth edition of the haemophilia B database lists in easily accessible form all known factor IX mutations due to small changes (base substitutions and short additions and/or deletions of < 30bp) identified in haemophilia B patients. The 1,142 patient entries are ordered by the nucleotide number of their mutation. Where known, details are given on: factor IX activity, factor IX antigen in circulation, and origin of mutation. References to published mutations are given and the laboratories generating the data are indicated.
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