Concepedia

Haemophilia B: database of point mutations and short additions and deletions

F. Giannelli, P. M. Green, KA High, JN Lozier, David Lillicrap, Michael Ludwig, K. Olek, Pieter H. Reitsma, M. Goossens, Akira Yoshioka,

Nucleic Acids Research · 1990 · 69 citations · 39 references

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References

39

Complete nucleotide sequences of the gene for human factor IX (antihemophilic factor B)

Shinji Yoshitake, Barbara G. Schach, Donald C. Foster et al. · Biochemistry · 1985 · 667 citations

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The first EGF‐like domain from human factor IX contains a high‐affinity calcium binding site.

Penny A. Handford, Martín Baron, Mark Mayhew et al. · The EMBO Journal · 1990 · 190 citations · Full text

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Defective propeptide processing of blood clotting factor IX caused by mutation of arginine to glutamine at position −4

A.K. Bentley · Cell · 1986 · 179 citations

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Molecular pathology of haemophilia B.

P. M. Green, D. R. Bentley, R. S. Mibashan et al. · The EMBO Journal · 1989 · 176 citations

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Direct detection of point mutations by mismatch analysis: application to haemophilia B

A.J. Montandon, P.M. Green, F. Giannelli et al. · Nucleic Acids Research · 1989 · 166 citations

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