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Gene Review

MMVP2  -  myxomatous mitral valve prolapse 2

Homo sapiens

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High impact information on MMVP2

  • Haplotype analysis across this region defines a 4.3-cM region between the markers D11S1923 and D11S1331 as the location of a new MVP locus, MMVP2, and confirms the genetic heterogeneity of this disorder [1].


  1. A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4. Freed, L.A., Acierno, J.S., Dai, D., Leyne, M., Marshall, J.E., Nesta, F., Levine, R.A., Slaugenhaupt, S.A. Am. J. Hum. Genet. (2003) [Pubmed]
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