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

Autor: Chamkha, Imen1, Mkaouar-Rebai, Emna1 emna_mkaouar@mail2world.com, Aloulou, Hajer2, Chabchoub, Imen2, Kifagi, Chamseddine3, Fendri-Kriaa, Nourhene1, Kammoun, Thouraya2, Hachicha, Mongia2, Fakhfakh, Faiza1
Zdroj: Biochemical & Biophysical Research Communications. Jan2011, Vol. 404 Issue 1, p504-510. 7p.
Databáze: Academic Search Ultimate
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