Defining the molecular genetic basis of idiopathic dilated cardiomyopathy

Trends in Cardiovascular Medicine

Volumn 7, Issue 2, 1997, Pages 60-63

  Olson, Timothy M ^a   Keating, Mark T ^b  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN;

AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME XP; CONGESTIVE CARDIOMYOPATHY; FAMILIAL DISEASE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; HUMAN; PRIORITY JOURNAL; REVIEW;

EID: 0030968021     PISSN: 10501738     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1050-1738(96)00139-9     Document Type: Review

References (30)

1. Ben-Yehuda O, Rockman HA: 1996. Regulation of myocardial contractility: insights from transgenic mice. Trends Cardiovasc Med 6:95-99.
2. Carlquist JF, Menlove RL, Murray MB, O'Connell JB, Anderson JL: 1991. HLA class II (DR and DQ) antigen associations in idiopathic dilated cardiomyopathy: validation study and meta-analysis of published HLA association studies. Circulation 83:515-522.
3. Chien KR: 1996. Genes and physiology: molecular physiology in genetically engineered animals. J Clin Invest 97:901-909.
4. Csanady M, Hogye M, Kallai A, Forster T, Szarazajtai T: 1995. Familial dilated cardiomyopathy: a worse prognosis compared with sporadic forms. Br Heart J 74:171-174.
5. Durand J-B, Bachinski LL, Bieling LC, et al.: 1995. Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32. Circulation 92:3387-3389.
6. Fadic R, Sunada Y, Waclawik AJ, et al.: 1996. Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy. N Engl J Med 334:362-366.
7. Gilbert EM, Bristow MR: 1994. Idiopathic dilated cardiomyopathy. In Hurst JW, ed. The Heart. New York, McGraw-Hill, pp 1609-1619.
8. Grompe M: 1993. The rapid detection of unknown mutations in nucleic acids. Nat Genet 5:111-117.
9. Kasper EK, Agema WRP, Hutchins GM, et al.: 1994. The causes of dilated cardiomyopathy: a clinicopathologic review of 673 consecutive patients. J Am Coll Cardiol 23:586-590.
10. Kass S, MacRae C, Graber HL, et al.: 1994. A gene that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1. Nat Genet 7:546-551.
11. Keating MT: 1995. Genetic approaches to cardiovascular disease: supravalvular aortic stenosis, Williams syndrome, and long-QT syndrome. Circulation 92:142-147.
12. Keeling PJ, Gang Y, Smith G, et al.: 1995. Familial dilated cardiomyopathy in the United Kingdom. Br Heart J 73:417-421.
13. Kelly DP, Strauss AW: 1994. Inherited cardiomyopathies. N Engl J Med 330:913-919.
14. Krajinovic M, Pinamonti B, Sinagra G, et al.: 1995. Linkage of familial dilated cardiomyopathy to chromosome 9. Am J Hum Genet 57:846-852.
15. Lifton RP: 1996. Molecular genetics of human blood pressure variation. Science 272:676-680.
16. Manolio TA, Baughman KL, Rodeheffer R, et al.: 1992. Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a national heart, lung, and blood institute workshop). Am J Cardiol 69:1458-1466.
17. McMinn TR, Ross J: 1995. Hereditary dilated cardiomyopathy. Clin Cardiol 18:7-15.
18. Michels VV: 1993. Genetics of idiopathic dilated cardiomyopathy. Heart Failure 9:87-94.
19. Michels VV, Moll PP, Miller FA, et al.: 1992. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. New Engl J Med 326:77-82.
20. Muntoni F, Cau M, Ganau A, et al.: 1993. Brief report: deletion of the dystrophin muscle-promoter region associated with x-linked dilated cardiomyopathy. N Engl J Med 329: 921-925.
21. Muntoni F, Wilson L, Marrosu G, et al.: 1995. A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart. J Clin Invest 96:693-699.
22. Oldfors A, Eriksson BO, Kyllerman M, Martinsson T, Wahlstrom J: 1994. Dilated cardiomyopathy and the dystrophin gene: an illustrated review. Br Heart J 72:344-348.
23. Olson TM, Keating MT: 1996. Mapping a cardiomyopathy locus to chromosome 3p22-p25. J Clin Invest 97:528-532.
24. Olson TM, Thibodeau SN, Lundquist PA, Schaid DJ, Michels VV: 1995. Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathy. J Med Genet 32:876-880.
25. kr potassium channel. Cell 81:299-307.
26. Towbin JA, Hejtmancik JF, Brink P, et al.: 1993. X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation 87:1854-1865.
27. Watkins H, Seidman JG, Seidman CE: 1995. Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy. Hum Mol Genet 4:1721-1727.
28. Weiss EJ, Bray PF, Tayback M, et al.: 1996. A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis. N Engl J Med 334:1090-1094.
29. Wiles HB, McArthur PD, Taylor AB, et al.: 1991. Prognostic features of children with idiopathic dilated cardiomyopathy. Am J Cardiol 68:1372-1376.
30. Zachara E, Caforio ALP, Carboni GP, et al.: 1993. Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families.