Corrigendum to “Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: Five novel mutations and review of the literature. Am J Med Genet Part A 2014 164A:2879–86”
Year: 2015
Type: erratum
Abstract: 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.
DOI: 10.1002/ajmg.a.37449
Institution: Seattle Children's Research Institute
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
OpenAlex ID: W2173035705