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Circulation
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Circulation. 2004;109:3258
doi: 10.1161/01.CIR.0000135150.43204.25
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(Circulation. 2004;109:3258.)
© 2004 American Heart Association, Inc.

Correction

In the article, "Hypertrophic Cardiomyopathy: Distribution of Disease Genes, Spectrum of Mutations, and Implications for a Molecular Diagnosis Strategy," by Richard et al, which appeared in the May 6, 2003, issue of the journal (Circulation. 2003;107:2227–2232), the authors regret that errors occurred in Tables 2 and 4Down. In Table 2, Exon 30, Nucleotide Change C19222T, the value listed under Coding Effect (E1377M) should be replaced with T1377M. In Table 4, row 3, the value listed under Troponin T (P120V) should be replaced with F110V. Also in Table 4, row 4, the value listed under Regulatory Light Chain (D166L) should be replaced with D166V. The corrected rows of Tables 2 and 4Down appear below.


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TABLE 2. MYH7 Mutations


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TABLE 4. Cardiac Troponin T, Cardiac Troponin I, and Regulatory and Essential Myosin Light Chain Mutations




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W. G. L. Kerrick, K. Kazmierczak, Y. Xu, Y. Wang, and D. Szczesna-Cordary
Malignant familial hypertrophic cardiomyopathy D166V mutation in the ventricular myosin regulatory light chain causes profound effects in skinned and intact papillary muscle fibers from transgenic mice
FASEB J, March 1, 2009; 23(3): 855 - 865.
[Abstract] [Full Text] [PDF]


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