S E Holmes, E O'Hearn, A Rosenblatt, C Callahan, H S Hwang, R G Ingersoll-Ashworth, A Fleisher, G Stevanin, A Brice, N T Potter, C A Ross & R L Margolis Nature Genet. 29, 377–378 (2001).
In the first sentence of the final paragraph, the locus 16q23.4 is incorrect. The corrected sentence is “Our results suggest that CAG/CTG repeat expansions of about 40 or more triplets at the HDL2 locus on 16q24.3 cause HDL2.”
In Fig. 2e, the cDNA that is labeled '(CTG)n=polyalanine' should be labeled: '(CTG)n=polyleucine'. The second to last sentence of the legend to Fig. 2 is missing a comma; the sentence should be: “Depending on the splice acceptor site, the repeat is in a 3′ untranslated region, in the frame to encode polyalanine, or in the frame to encode polyleucine.”
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The online version of the original article can be found at 10.1038/ng760
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Correction: A CTG trinucleotide repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease–like 2. Nat Genet 30, 123 (2002). https://doi.org/10.1038/ng0102-123a
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DOI: https://doi.org/10.1038/ng0102-123a
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