Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family – CORRIGENDUM

Mohammad Mahdavi; Neda Mohsen-Pour; Majid Maleki; Mahshid Hesami; Niloofar Naderi; Golnaz Houshmand; Hamid R. Rasouli Jazi; Hossein Shahzadi; Samira Kalayinia

doi:10.1017/S1047951121004832

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

Hamid R. Rasouli Jazi ,

Hossein Shahzadi and

Samira Kalayinia

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Abstract

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Type: Corrigendum
Information: Cardiology in the Young , Volume 32 , Issue 9 , September 2022 , pp. 1468

DOI: https://doi.org/10.1017/S1047951121004832 [Opens in a new window]
Copyright: © The Author(s), 2021. Published by Cambridge University Press

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.

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 CrossRef Google Scholar