PUBLICATION
CORRECTION 2: Rare and de novo coding variants in chromodomain genes in Chiari I malformation
- Authors
- Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A.T., Gannon, S.R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Brunetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A., Garrett, M.E., Soldano, K., Macaya, A., Conrad, D., Strahle, J., Dobbs, M.B., Turner, T.N., Shannon, C.N., Brockmeyer, D., Limbrick, D.D., Gurnett, C.A., Haller, G.
- ID
- ZDB-PUB-220906-237
- Date
- 2021
- Source
- American journal of human genetics 108: 530-531 (Other)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 33667397 Full text @ Am. J. Hum. Genet.
Citation
Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A.T., Gannon, S.R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Brunetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A., Garrett, M.E., Soldano, K., Macaya, A., Conrad, D., Strahle, J., Dobbs, M.B., Turner, T.N., Shannon, C.N., Brockmeyer, D., Limbrick, D.D., Gurnett, C.A., Haller, G. (2021) CORRECTION 2: Rare and de novo coding variants in chromodomain genes in Chiari I malformation. American journal of human genetics. 108:530-531.
Abstract
(The American Journal of Human Genetics 108, 100–114; January 7, 2021)
Three variants were misnamed in the text and mislabeled in Figure 2. The relevant sentence has been changed to read, “The three de novo CHD8 mutations observed in CM1 include two stop-gain mutations (GenBank: NM_001170629.2; c.4414C>T [p.Arg1472∗] and c.4514G>A [p.Trp1505∗]) and a splice donor site mutation (c.2907+1G>T [p.?]).” These errors have been corrected online. The authors apologize for these errors.
Errata / Notes
This article corrects ZDB-PUB-201223-9 .
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping