Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews

This publication has 13 references indexed in Scilit:

• Origins of Old Testament priests
  Nature, 1998
• Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes
  American Journal of Human Genetics, 1998
• The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin.
  1997
• Launching Microsatellites: A Review of Mutation Processes and Methods of Phylogenetic Inference
  Journal of Heredity, 1997
• Estimating the age of alleles by use of intraallelic variability.
  1997
• Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population
  Nature Genetics, 1995
• One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.
  1995
• Mutation of human short tandem repeats
  Human Molecular Genetics, 1993
• FAILURE TO DETECT VARIANT (CRM+) PLASMA THROMBOPLASTIN ANTECEDENT (FACTOR-XI) MOLECULES IN HEREDITARY PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCY - A STUDY OF 125 PATIENTS OF SEVERAL ETHNIC BACKGROUNDS
  1985
• HIGH GENE FREQUENCY OF FACTOR-XI (PTA) DEFICIENCY IN ASHKENAZI JEWS
  1978