Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

(American Journal of Human Genetics 95, 611–621; November 6, 2014)

In this article, mutation c.1894+1G>A in Table 1 and on page 616 is incorrect and should have been c.1894+1G>T, as correctly written in Figure 2. In addition, Figure 2C incorrectly shows that c.1894+1G>T occurs in intron 17. The correct intron is 19, as noted on page 616. A revised Figure 2 appears below. The authors apologize for the errors.

Figure 2.

Identification of SNX14 Mutations in Three Affected Families