Article
Haplotype sharing test maps genes for familial cardiomyopathies.
Clinical genetics - 1 May 2011
van der Zwaag P A, van Tintelen J P, Gerbens F, Jongbloed J D H, Boven L G, van der Smagt J J, van der Roest W P, van Langen I M, Bikker H, Hauer R N W, van den Berg M P, Hofstra R M W, te Meerman G J
Abstract excerpt
Identifying a mutation in a heterogeneous disease such as inherited cardiomyopathy is a challenge because classical methods, like linkage analysis, can often not be applied as there are too few meioses between affected individuals. However, if affected individuals share the same causal mutation,...
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