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PDFNeurogenetics
Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation
- Correspondence to Dr Alistair T Pagnamenta, Wellcome Centre for Human Genetics, Oxford University, Oxford, Oxfordshire, UK; alistair{at}well.ox.ac.uk
Citation
Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation
Publication history
- Received October 17, 2020
- Revised December 23, 2020
- Accepted January 10, 2021
- First published February 5, 2021.
Online issue publication
March 23, 2022
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© Author(s) (or their employer(s)) 2022. 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/.