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Neurology: Genetics logoLink to Neurology: Genetics
. 2019 Feb 4;5(1):e311. doi: 10.1212/NXG.0000000000000311

The complex structure of ATXN2 genetic variation

PMCID: PMC6384013  PMID: 30842977

In the editorial, “The complex structure of ATXN2 genetic variation,” by Pulst1, first published online December 6, 2018, the reference for Tojima et al.’s article should read: 1. Tojima M, Murakami G, Hikawa R, et al. Homozygous 31 trinucleotide repeats in the SCA2 allele are pathogenic for cerebellar ataxia. Neurol Genet 2018;4:e283. DOI: 10.1212/NXG.0000000000000283. The publisher regrets the error.

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