The authors apologise that upon publication the accession number was incorrectly listed.
The correct accession number is: NM_001267550.2(TTN):c.[62674G>A];[68984A>C].
The online version of this article has been updated.
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Article contents
Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family – CORRIGENDUM
Published online by Cambridge University Press: 06 December 2021
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- Corrigendum
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- © The Author(s), 2021. Published by Cambridge University Press
References
Mahdavi, M., Mohsen-Pour, N., Maleki, M., Hesami, M., Naderi, N., Houshmand, G., … Kalayinia, S. (2021). in an Iranian family. Cardiology in the Young, 1–6. doi: 10.1017/S1047951121004455
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