Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01732.x/fullpdf
Reference28 articles.
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2. 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.;Shpilberg;Blood,1995
3. Factor XI deficiency in humans.;Seligsohn;J Thromb Haemost,2009
4. Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4.;Kato;Cytogenet Cell Genet,1989
5. Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis tools.;Saunders;Hum Mutat,2005
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