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A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.
Posch MG, Posch MJ, Geier C, Erdmann B, Mueller W, Richter A, Ruppert V, Pankuweit S, Maisch B, Perrot A, Buttgereit J, Dietz R, Haverkamp W, Ozcelik C. Posch MG, et al. Among authors: perrot a. Mol Genet Metab. 2008 Sep-Oct;95(1-2):74-80. doi: 10.1016/j.ymgme.2008.06.005. Epub 2008 Aug 3. Mol Genet Metab. 2008. PMID: 18678517
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
Geier C, Gehmlich K, Ehler E, Hassfeld S, Perrot A, Hayess K, Cardim N, Wenzel K, Erdmann B, Krackhardt F, Posch MG, Osterziel KJ, Bublak A, Nägele H, Scheffold T, Dietz R, Chien KR, Spuler S, Fürst DO, Nürnberg P, Ozcelik C. Geier C, et al. Among authors: perrot a. Hum Mol Genet. 2008 Sep 15;17(18):2753-65. doi: 10.1093/hmg/ddn160. Epub 2008 May 27. Hum Mol Genet. 2008. PMID: 18505755
Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathy.
Ruppert V, Meyer T, Struwe C, Petersen J, Perrot A, Posch MG, Ozcelik C, Richter A, Maisch B, Pankuweit S; German Heart Failure Network. Ruppert V, et al. Among authors: perrot a. Eur J Hum Genet. 2010 Jun;18(6):694-9. doi: 10.1038/ejhg.2010.3. Epub 2010 Feb 10. Eur J Hum Genet. 2010. PMID: 20145677 Free PMC article.
[Familial dilated cardiomyopathy].
Osterziel KJ, Hassfeld S, Geier C, Perrot A. Osterziel KJ, et al. Among authors: perrot a. Herz. 2005 Sep;30(6):529-34. doi: 10.1007/s00059-005-2732-3. Herz. 2005. PMID: 16170685 Review. German.
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.
Perrot A, Sigusch HH, Nägele H, Genschel J, Lehmkuhl H, Hetzer R, Geier C, Leon Perez V, Reinhard D, Dietz R, Josef Osterziel K, Schmidt HH. Perrot A, et al. Eur J Heart Fail. 2006 Aug;8(5):484-93. doi: 10.1016/j.ejheart.2005.11.004. Epub 2006 Jan 4. Eur J Heart Fail. 2006. PMID: 16386954 Free article.
348 results