De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

Volume: 105, Issue: 3, Pages: 672 - 674
Published: Sep 1, 2019
Abstract
(The American Journal of Human Genetics 105, 413–424; August 1, 2019) In the originally published version of this article, Figures 3B and 3C included the allele name “sisy” but the correct term is “wrd37,” as appears in the rest of the article. In addition, there are two edits in Figure 3A: Thr125 has been highlighted instead of Thr124 and “Patient variants” has been changed to “Protein variants.” All these changes are reflected in the figure...
Paper Details
Title
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
Published Date
Sep 1, 2019
Volume
105
Issue
3
Pages
672 - 674
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