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Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.
Mogensen J, Perrot A, Andersen PS, Havndrup O, Klausen IC, Christiansen M, Bross P, Egeblad H, Bundgaard H, Osterziel KJ, Haltern G, Lapp H, Reinecke P, Gregersen N, Børglum AD. Mogensen J, et al. Among authors: haltern g. J Med Genet. 2004 Jan;41(1):e10. doi: 10.1136/jmg.2003.010447. J Med Genet. 2004. PMID: 14729850 Free PMC article. No abstract available.
Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.
Scheffold T, Kullmann S, Huge A, Binner P, Ochs HR, Schöls W, Thale J, Motz W, Hegge FJ, Stellbrink C, Dorsel T, Gülker H, Heuer H, Dinh W, Stoll M, Haltern G; Forschungsverbund Herz-Kreislauf in NRW (Research Consortium Heart and Circulation in North Rhine-Westphalia). Scheffold T, et al. Among authors: haltern g. BMC Cardiovasc Disord. 2011 Mar 7;11:9. doi: 10.1186/1471-2261-11-9. BMC Cardiovasc Disord. 2011. PMID: 21385355 Free PMC article.
21 results