Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss

Mitochondrial DNA mutations play an important role in causing sensorineural hearing loss. The purpose of this study was to determine the association of the mitochondrial genes RNR1, MT-TL1, and ND1 as well as the nuclear genes GJB2 and GJB6 with audiological examinations in nonfamilial Iranians with...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Ther Clin Risk Manag
Päätekijät: Balali, Maryam, Kamalidehghan, Behnam, Farhadi, Mohammad, Ahmadipour, Fatemeh, Ashkezari, Mahmoud Dehghani, Hemami, Mohsen Rezaei, Arabzadeh, Hossein, Falah, Masoumeh, Meng, Goh Yong, Houshmand, Massoud
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Dove Medical Press 2016
Aiheet:
Original Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4743636/
https://ncbi.nlm.nih.gov/pubmed/26889084
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TCRM.S90581
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