The factor IX gene as a model for analysis of human germline mutations: an update

Author:

Sommer Steve S.,Ketterling Rhett P.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference107 articles.

1. Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in the human gene;Koeberl;Am. J. Hum. Genet.,1990

2. The incidence and distribution of CpG"TpG transitions in the coagulation factor IX gene;Green;Nucleic Acids Res.,1990

3. Assessing the underlying pattern of human germline mutations: lessons from the factor IX gene;Sommer;FASEB J.,1992

4. Germline origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutation;Ketterling;Am. J. Hum. Genet.,1993

5. First report on UK database of haemophilia B mutations and pedigrees;Saad;Thromb. Haemost.,1994

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