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  1. 1
    Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family

    Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family von Mahdavi, Mohammad, Mohsen-Pour, Neda, Maleki, Majid, Hesami, Mahshid, Naderi, Niloofar, Houshmand, Golnaz, Rasouli Jazi, Hamid R., Shahzadi, Hossein, Kalayinia, Samira

    Veröffentlicht in Cardiology in the young

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

    Whole -exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family - CORRIGENDUM von Mahdavi, Mohammad, Mohsen-Pour, Neda, Maleki, Majid, Hesami, Mahshid, Naderi, Niloofar, Houshmand, Golnaz, Rasouli Jazi, Hamid R, Shahzadi, Hossein, Kalayinia, Samira

    Veröffentlicht in Cardiology in the young

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