Corrigendum to “Congenital microcephaly and chorioretinopathy due to de novo heterozygousKIF11mutations: Five novel mutations and review of the literature. Am J Med Genet Part A 2014 164A:2879-86”

In Tables I and II in the article, there are a few errors in the genomic coordinates and mutation nomenclature. Revised Table II lists the mutations with the correct nomenclature. Supplementary Figure I shows representative Sanger sequencing chromatograms of these mutations. The authors regret these errors. These mutations have been submitted to the LOVD KIF11 database (http://databases.lovd.nl/shared/variants/KIF11). The individual IDs of these mutations are 47821, 47847, 47849, 47850 and 47851. Additional supporting information may be found in the online version of this article at the publisher's web-site. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.