Article info
PDFNovel disease loci
Short report
De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features
- Correspondence to Dr Alka Malhotra, Illumina Inc., San Diego, CA 92122, USA; amalhotra{at}illumina.com
Citation
De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features
Publication history
- Received April 24, 2020
- Revised July 7, 2020
- Accepted July 14, 2020
- First published August 20, 2020.
Online issue publication
January 08, 2022
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© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.