Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-17T23:41:27.980Z Has data issue: false hasContentIssue false
  • English
  • Français

Identification of specific genes involved in schizophrenia aetiology – what difference does it make? – CORRIGENDUM

Published online by Cambridge University Press:  23 May 2022

David Curtis
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content. As you have access to this content, full HTML content is provided on this page. A PDF of this content is also available in through the ‘Save PDF’ action button.

Keywords

SchizophreniagenesexomeNMDA receptorSETD1A
Type
Corrigendum
Information
The British Journal of Psychiatry , Volume 221 , Issue 2 , August 2022 , pp. 495
Check for updates
Copyright
Copyright © The Author(s), 2022. Published by Cambridge University Press on behalf of the Royal College of Psychiatrists

The author would like to update the citation of a pre-print in the references to the full citation. The full citation of reference 1 should read:

Singh T, on behalf of the Schizophrenia Exome Meta-analysis (SCHEMA) Consortium. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 2022; 604: 509–516. https://doi.org/10.1038/s41586-022-04556-w

The author and Publisher apologise for this error.

References

Curtis, D. Identification of specific genes involved in schizophrenia aetiology – what difference does it make? The British Journal of Psychiatry 2022; 1–3. doi: 10.1192/bjp.2021.153.Google Scholar
Singh, T, on behalf of the Schizophrenia Exome Meta-analysis (SCHEMA) Consortium. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 2022; 604: 509–516. https://doi.org/10.1038/s41586-022-04556-wCrossRefGoogle Scholar
Submit a response

eLetters

No eLetters have been published for this article.