Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

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Nat. Genet. 38, 93–100 (2006); published online 27 November 2005; corrected after print 30 June 2006

In the version of this article initially published, the numbering of references 22–29 in the reference list was incorrect. The correct numbering is as follows:

22. Watkins, D. Cobalamin metabolism in methionine-dependent human tumour and leukemia cell lines. Clin. Invest. Med. 21, 151–158 (1998).

23. Watkins, D., Matiaszuk, N. & Rosenblatt, D.S. Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH). J. Med. Genet. 37, 510–513 (2000).

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27. Yao, J. & Shoubridge, E.A. Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome C oxidase deficiency. Hum. Mol. Genet. 8, 2541–2549 (1999).

The error has been corrected in the PDF version of this article.

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The online version of the original article can be found at 10.1038/ng1683

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Lerner-Ellis, J., Tirone, J., Pawelek, P. et al. Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type. Nat Genet 38, 957 (2006) doi:10.1038/ng0806-957a

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