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Year | Number of Results |
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2006 | 1 |
2007 | 1 |
2009 | 1 |
2010 | 1 |
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Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease.
Eur Heart J. 2007 Mar;28(5):581-8. doi: 10.1093/eurheartj/ehl380. Epub 2006 Nov 14.
Eur Heart J. 2007.
PMID: 17105751
De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy.
Klauke B, Kossmann S, Gaertner A, Brand K, Stork I, Brodehl A, Dieding M, Walhorn V, Anselmetti D, Gerdes D, Bohms B, Schulz U, Zu Knyphausen E, Vorgerd M, Gummert J, Milting H.
Klauke B, et al.
Hum Mol Genet. 2010 Dec 1;19(23):4595-607. doi: 10.1093/hmg/ddq387. Epub 2010 Sep 9.
Hum Mol Genet. 2010.
PMID: 20829228
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Sporadic arrhythmogenic right ventricular cardiomyopathy/dysplasia due to a de novo mutation.
Gandjbakhch E, Fressart V, Bertaux G, Faivre L, Simon F, Frank R, Fontaine G, Villard E, Coirault C, Hainque B, Charron P.
Gandjbakhch E, et al.
Europace. 2009 Mar;11(3):379-81. doi: 10.1093/europace/eun378. Epub 2009 Jan 16.
Europace. 2009.
PMID: 19151369
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