Erratum: Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy (Journal of Molecular Medicine (2005) 83 (468-477) DOI: 10.1007/s00109-005-0635-7);Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy

Journal of Molecular Medicine

Volumn 83, Issue 6, 2005, Pages 468-477

  Perrot, Andreas ^a   Schmidt Traub, Hajo ^a   Hoffmann, Bernard ^a   Prager, Matthias ^a   Bit Avragim, Nana ^a   Rudenko, Raisa I ^b   Usupbaeva, Dinara A ^b   Kabaeva, Zhyldyz ^a   Imanov, Bakytbek ^b   Mirrakhimov, Mirsaid M ^b   Dietz, Rainer ^a   Wycisk, Anna ^c   Tendera, Michal ^c   Geßner, Reinhard ^a   Osterziel, Karl Josef ^a,d  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b National Center for Cardiology and Internal Medicine   (Kyrgyzstan)

^c MEDICAL UNIVERSITY OF SILESIA   (Poland)

^d Silesian School of Medicine ^*

Author keywords

Beta myosin heavy chain gene; Genotype phenotype correlations; Hypertrophic cardiomyopathy

Indexed keywords

MYOSIN HEAVY CHAIN;

ADOLESCENT; ADULT; ARTICLE; AUTOMATION; CHILD; CONTROLLED STUDY; CORRELATION ANALYSIS; DIAGNOSTIC PROCEDURE; DNA DETERMINATION; FAMILY; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENOTYPE; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATION RATE; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; PREVALENCE; RISK ASSESSMENT; SCREENING; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 21544439840     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00109-005-0722-9     Document Type: Erratum

References (28)

1. Ciro E (1983) Heterogeneous morphologic expression of genetically transmitted hypertrophic cardiomyopathy: two-dimensional echocardiographic analysis. Circulation 67:1227-1233
2. Maron BJ, Bonow RO, Seshagiri TNR, Roberts WC, Epstein SE (1981) Hypertrophic cardiomyopathy with ventricular septal hypertrophy localized to the apical region of the left ventricle. Am J Cardiol 49:1838-1848
3. Roberts R, Sigwart U (2001) New concepts in hypertrophic cardiomyopathy, part I. Circulation 104:2113-2116
4. Maron BJ (2002) Hypertrophic cardiomyopathy: a systematic review. JAMA 287:1308-1320
5. Seidman JG, Seidman C (2001) The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell 104:557-567
6. Marian AJ, Roberts R (2001) The molecular genetic basis for hypertrophic cardiomyopathy. J Mol Cell Cardiol 33:655-670
7. Jaenicke T, Diederich KW, Haas W, Schleich J, Lichter P, Pfordt M, Bach A, Vosberg HP (1990) The complete sequence of the human b-myosin heavy chain gene and a comparative analysis of its product. Genomics 8:194-206
8. Ackerman MJ, Van Driest SL, Ommen SR, Will ML, Nishimura RA, Tajik AJ, Gersh BJ (2002) Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin t genes in hypertrophic cardiomyopathy. J Am Coll Cardiol 39:2042-2048
9. Richardson P, McKenna W, Bristow M, Maisch B, Mautner B, O'Connel J, Olsen EGJ, Thiene G, Guyarfas I (1996) Report of the 1995 WHO/ISFC Task Force on the definition and classification of cardiomyopathies. Circulation 93:841-842
10. McKenna WJ, Spirito P, Desnos M, Dubourg O, Komajda M (1997) Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families. Heart 77:130-132
11. Sahn DJ, DeMaria A, Kisslo J, Weyman A (1978) The Committee on M-mode standardization of the American Society of Echocardiography: recommendations regarding quantitation in M-mode echocardiography: results of a survey of echocardiographic measurements. Circulation 58:1072-1083
12. Lahiri DK, Nurnberger JI (1991) A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies. Nucleic Acids Res 19:5444
13. Jääskeläinen P, Soranta M, Miettinen R, Saarinen L, Pihlajamäki J, Silvennoinen K, Tikanoja T, Laakso M, Kuusisto J (1998) The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population. J Am Coll Cardiol 32:1709-1716
14. Mörner S, Richard P, Kazzam E, Hellman U, Hainque B, Schwartz K, Waldenström A (2003) Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden. J Mol Cell Cardiol 35:841-849
15. Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichreau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M (2003) Hypertrophic cardiomyopathy - distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 107:2227-2232
16. Van Driest SL, Jaeger MA, Ommen SR, Will ML, Gersh BJ, Tajik AJ, Ackerman MJ (2004) Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy. J Am Coll Cardiol 44:602-610
17. Erdmann J, Daehmlow S, Wischke S, Senyuwa M, Werner U, Raible J, Tanis N, Dyachenko S, Hummel M, Hetzer R, Regitz-Zagrosek V (2003) Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy. Clin Genet 64:339-349
18. Hougs L, Havndrup O, Bundgaard H, Kober L, Vuust J, Larsen LA, Christiansen M, Andersen PS (2005) One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod region. Eur J Hum Genet 13:161-165
19. Hoffmann B, Schmidt-Traub H, Perrot A, Osterziel KJ, Geßner R (2001) First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy. Human Mutat 17:524
20. Geier C, Perrot A, Özcelik C, Binner P, Counsell D, Hoffmann K, Pilz B, Martiniak Y, Gehmlich K, van der Ven PFM, Fürst DO, Vornwald A, von Hodenberg E, Nürnberg P, Scheffold T, Dietz R, Osterziel KJ (2003) Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy. Circulation 107:1390-1395
21. Vidal-Puig A, Moller DE (1994) Comparative sensitivity of alternative single-strand conformation polymorphism (SSCP) methods. Biotechniques 17:490-496
22. Jordanova A, Kalaydjieva L, Savov A, Claustres M, Schwarz M, Estivill X, Angelicheva D, Haworth A, Casals T, Kremensky I (1997) SSCP analysis: a blind sensitivity trail. Human Mutat 10:65-70
23. Fananapazir L, Dalakas MC, Cyran F, Cohn G, Epstein ND (1993) Missense mutations in the beta-myosin heavy chain gene cause central core disease in hypertrophic cardiomyopathy. Proc Natl Acad Sci USA 90:3993-3997
24. Woo A, Rakowski H, Liew JC, Zhao MS, Liew CC, Parker TG, Zeller M, Wigle ED, Sole MJ (2003) Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis. Heart 89:1179-1185
25. Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, McKenna W, Kristinsson A, Roberts R, Sole M, Maron BJ, Seidman JG, Seidman CE (1998) Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med 338:1248-1257
26. Arad M, Seidman JG, Seidman CE (2002) Phenotypic diversity in hypertrophic cardiomyopathy. Hum Mol Genet 11:2499-2506
27. Blair E, Redwood C, Oliveira M, Moolman-Smook JC, Brink P, Corfield VA, Östman-Smith I, Watkins H (2002) Mutations in the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy. Circ Res 90:263-269
28. Lowey S (2002) Functional consequences of mutations in the myosin heavy chain at sites implicated in familial hypertrophic cardiomyopathy. Trends Cardiovasc Med 12:348-354