Article info
PDFCase Reports: Rare disease
Mutation of the MYL3 gene in a patient with mid-ventricular obstructive hypertrophic cardiomyopathy
- Correspondence to Dr Akash Mavilakandy; am1138{at}leicester.ac.uk
Citation
Mutation of the MYL3 gene in a patient with mid-ventricular obstructive hypertrophic cardiomyopathy
Publication history
- Accepted February 8, 2022
- First published March 14, 2022.
Online issue publication
January 23, 2023
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© BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.