A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss

Imen Chamkha, Emna Mkaouar-Rebai, Hajer Aloulou, Imen Chabchoub, Chamseddine Kifagi, Nourhene Fendri-Kriaa, Thouraya Kammoun, Mongia Hachicha, Faiza Fakhfakh

Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

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Biochemistry, Genetics and Molecular Biology