The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms
- PMID: 11239412
- DOI: 10.1016/s0092-8674(01)00242-2
The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms
Similar articles
-
[Recommendations for gene assays for cardiomyopathy in children].Zhonghua Er Ke Za Zhi. 2013 Aug;51(8):595-7. Zhonghua Er Ke Za Zhi. 2013. PMID: 24225290 Chinese. No abstract available.
-
[Heart failure as genetic disease: exemplified by cardiomyopathy].Internist (Berl). 1993 Oct;34(10):902-11. Internist (Berl). 1993. PMID: 8225839 Review. German. No abstract available.
-
[Genetic screening of cardiomyopathies].Z Kardiol. 2000 Jul;89(7):638-40. doi: 10.1007/s003920070215. Z Kardiol. 2000. PMID: 10957791 German.
-
Molecular diagnosis of myocardial disease.Expert Rev Mol Diagn. 2002 Nov;2(6):587-602. doi: 10.1586/14737159.2.6.587. Expert Rev Mol Diagn. 2002. PMID: 12465455 Review.
-
Molecular diagnostics of cardiomyopathies: the future is here.Circ Cardiovasc Genet. 2011 Apr;4(2):103-4. doi: 10.1161/CIRCGENETICS.110.959247. Circ Cardiovasc Genet. 2011. PMID: 21505198 No abstract available.
Cited by
-
Hypertrophic cardiomyopathy: Mutations to mechanisms to therapies.Front Physiol. 2022 Sep 26;13:975076. doi: 10.3389/fphys.2022.975076. eCollection 2022. Front Physiol. 2022. PMID: 36225299 Free PMC article. Review.
-
TNNT2 gene polymorphisms are associated with susceptibility to idiopathic dilated cardiomyopathy in the Han Chinese population.Biomed Res Int. 2013;2013:201372. doi: 10.1155/2013/201372. Epub 2013 Mar 17. Biomed Res Int. 2013. PMID: 23586019 Free PMC article.
-
PRKAG2 mutation: An easily missed cardiac specific non-lysosomal glycogenosis.Ann Pediatr Cardiol. 2015 May-Aug;8(2):153-6. doi: 10.4103/0974-2069.154149. Ann Pediatr Cardiol. 2015. PMID: 26085771 Free PMC article.
-
Cardiac-specific deletion of the microtubule-binding protein CENP-F causes dilated cardiomyopathy.Dis Model Mech. 2012 Jul;5(4):468-80. doi: 10.1242/dmm.008680. Epub 2012 Mar 22. Dis Model Mech. 2012. PMID: 22563055 Free PMC article.
-
Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.J Mol Med (Berl). 2005 Jun;83(6):468-77. doi: 10.1007/s00109-005-0635-7. Epub 2005 Apr 22. J Mol Med (Berl). 2005. PMID: 15856146
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical