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

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Bibliographic Details
Published in:Cardiology in the young 2022-09, Vol.32 (9), p.1-1468
Main Authors: Mahdavi, Mohammad, Mohsen-Pour, Neda, Maleki, Majid, Hesami, Mahshid, Naderi, Niloofar, Houshmand, Golnaz, Rasouli Jazi, Hamid R, Shahzadi, Hossein, Kalayinia, Samira
Format: Article
Language:English
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ISSN:1047-9511
1467-1107
DOI:10.1017/S1047951121004832