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. 2013 Oct;21(10).
doi: 10.1038/ejhg.2012.276. Epub 2012 Dec 19.

Clinical utility gene card for: dilated cardiomyopathy (CMD)

Anna Posafalvi  1 , Johanna C Herkert, Richard J Sinke, Maarten P van den Berg, Jens Mogensen, Jan D H Jongbloed, J Peter van Tintelen
Affiliations

Clinical utility gene card for: dilated cardiomyopathy (CMD)

Anna Posafalvi et al. Eur J Hum Genet. 2013 Oct.
No abstract available

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References

    1. Herman DS, Lam L, Taylor MR, et al. Truncations of titin causing dilated cardiomyopathy. N Engl J Med. 2012;366:619–628. - PMC - PubMed
    1. Muntoni F, Cau M, Ganau A, et al. Brief report: deletion of the dystrophin muscle-promoter region addociated with X-linked dilated cardiomyopathy. N Engl J Med. 1993;329:921–925. - PubMed
    1. Towbin JA, Hejtmancik JF, Brink P, et al. X-linked dilated cardiomyopathy Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation. 1993;87:1854–1865. - PubMed
    1. van Tintelen JP, Tio RA, Kerstjens-Frederikse WS, et al. Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene. J Am Coll Cardiol. 2007;49:2430–2439. - PubMed
    1. Norton N, Li D, Rieder MJ, et al. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. Am J Hum Genet. 2011;88:273–282. - PMC - PubMed

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