Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025))

Elisabeth M. Lodder, Pasquelena De Nittis, Charlotte D. Koopman, Wojciech Wiszniewski, Carolina Fischinger Moura de Souza, Najim Lahrouchi, Nicolas Guex, Valerio Napolioni, Federico Tessadori, Leander Beekman, Eline A. Nannenberg, Lamiae Boualla, Nico A. Blom, Wim de Graaff, Maarten Kamermans, Dario Cocciadiferro, Natascia Malerba, Barbara Mandriani, Zeynep Hande Coban Akdemir, Richard J. FishMohammad K. Eldomery, Ilham Ratbi, Arthur A.M. Wilde, Teun de Boer, William F. Simonds, Marguerite Neerman-Arbez, V. Reid Sutton, Fernando Kok, James R. Lupski, Alexandre Reymond, Connie R. Bezzina, Jeroen Bakkers, Giuseppe Merla

Research output: Contribution to journalComment/debate

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Abstract

(The American Journal of Human Genetics 99, 704–710; September 1, 2016) 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.

Original languageEnglish (US)
Number of pages1
JournalAmerican Journal of Human Genetics
Volume99
Issue number3
DOIs
StatePublished - Sep 1 2016

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ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

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., ... Merla, G. (2016). Erratum: GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability (American Journal of Human Genetics (2016) 99(3) (704–710)(S0002929716302294)(10.1016/j.ajhg.2016.06.025)). American Journal of Human Genetics, 99(3). https://doi.org/10.1016/j.ajhg.2016.08.011