Test of rare variant association based on affected sib-pairs
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg201443.pdf
Reference33 articles.
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3. Marini NJ, Gin J, Ziegle J et al: The prevalence of folate-remedial MTHFR enzyme variants in humans. Proc Natl Acad Sci USA 2008; 105: 8055–8060.
4. Ji W, Foo JN, O'Roak BJ et al: Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet 2008; 40: 592–599.
5. Cohen JC, Pertsemlidis A, Fahmi S et al: Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma lowdensity lipoprotein levels. Proc Natl Acad Sci USA 2006; 103: 1810–1815.
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