Genet Med advance online publication 28 December 2017; doi:10.1038/gim.2017.203
Correction to: Genet Med (2017) 19, 1144–1150 doi:https://doi.org/10.1038/gim.2017.22
In the published version of this article, the legends for the Supplementary Figures were missing. The legends appear below. The authors regret the error.
Supplementary Figure S1. Pedigrees of families reported in this study. Note the consanguineous nature of all pedigrees. The genotypes for the identified recessive variants are shown in red under each symbol.
Supplementary Figure S2. Homology model of the GABRD molecule, established based on the 50% identical PDB entry 4cof (QMEAN score −2.03). The five chains that form the pentameric channel are color-coded. Thr292, located in the helical transmembrane channel domain, is shown in green. Left: side view. Right: view into the channel, orientation toward the cytoplasm.
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The online version of the original article can be found at https://doi.org/10.1038/gim.2017.22
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Monies, D., Maddirevula, S., Kurdi, W. et al. Correction: Corrigendum: Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation. Genet Med 20, 380 (2018). https://doi.org/10.1038/gim.2017.203
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DOI: https://doi.org/10.1038/gim.2017.203
