Population
43 individuals from a large family segregating autosomal dominant mitral valve prolapse
Design
Other
Authors
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May facilitate early gene carrier identification in families; leaves open the causal variant at this locus.
Mapping a new locus (MMVP3) for autosomal dominant mitral valve prolapse to chromosome 13q31.3-q32.1 confirms genetic heterogeneity and may help identify early gene carriers.
Nesta et al. (2005) studied this question.
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