PUBLICATION
CORRECTION: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
- Authors
- Lodder, E.M., De Nittis, P., Koopman, C.D., Wiszniewski, W., Moura de Souza, C.F., Lahrouchi, N., Guex, N., Napolioni, V., Tessadori, F., Beekman, L., Nannenberg, E.A., Boualla, L., Blom, N.A., de Graaff, W., Kamermans, M., Cocciadiferro, D., Malerba, N., Mandriani, B., Coban Akdemir, Z.H., Fish, R.J., Eldomery, M.K., Ratbi, I., Wilde, A.A.M., de Boer, T., Simonds, W.F., Neerman-Arbez, M., Sutton, V.R., Kok, F., Lupski, J.R., Reymond, A., Bezzina, C.R., Bakkers, J., Merla, G.
- ID
- ZDB-PUB-220906-53
- Date
- 2016
- Source
- American journal of human genetics 99: 786 (Other)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 27588455 Full text @ Am. J. Hum. Genet.
Citation
Lodder, E.M., De Nittis, P., Koopman, C.D., Wiszniewski, W., Moura de Souza, C.F., Lahrouchi, N., Guex, N., Napolioni, V., Tessadori, F., Beekman, L., Nannenberg, E.A., Boualla, L., Blom, N.A., de Graaff, W., Kamermans, M., Cocciadiferro, D., Malerba, N., Mandriani, B., Coban Akdemir, Z.H., Fish, R.J., Eldomery, M.K., Ratbi, I., Wilde, A.A.M., de Boer, T., Simonds, W.F., Neerman-Arbez, M., Sutton, V.R., Kok, F., Lupski, J.R., Reymond, A., Bezzina, C.R., Bakkers, J., Merla, G. (2016) CORRECTION: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. American journal of human genetics. 99:786.
Abstract
In the originally published version of this paper, several cells in Table 1 were incorrect. “Lexical production” has now been revised from “nonverbal” to “delayed” for both individuals in family E, and “light RV dilatation” has now been deleted from the “Heart structural abnormalities” row for individual II.1 in family E. Additionally, all instances of “NR” and “NT” (for “not reported” and “not tested”) have been revised to “NA” (for “not available”) throughout. The table is now correct both online and in print. The authors regret these errors and any confusion that might have resulted. Finally, due to technical error, the Supplemental Data file was not complete in the originally published version but now includes all relevant supplemental figures and tables.
Errata / Notes
This article corrects ZDB-PUB-160816-8.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping