Article info
PDFDevelopmental defects
Original research
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes
- Correspondence to Dr Mustafa K Khokha, Pediatric Genomics Discovery Program, Department of Pediatrics and Genetics, Yale University School of Medicine, New Haven, CT 06510, USA; mustafa.khokha{at}yale.edu
Citation
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes
Publication history
- Received December 23, 2019
- Revised May 1, 2020
- Accepted May 25, 2020
- First published July 6, 2020.
Online issue publication
January 10, 2022
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© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.