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The contribution of the mitochondrial COI/tRNASer(UCN) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients

✍ Scribed by Małgorzata Rydzanicz; Karolina Cywińska; Maciej Wróbel; Agnieszka Pollak; Wojciech Gawęcki; Irena Wojsyk-Banaszak; Urszula Lechowicz; Małgorzata Mueller-Malesińska; Monika Ołdak; Rafał Płoski; Henryk Skarżyński; Krzysztof Szyfter; Witold Szyfter

Book ID: 116989350
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 874 KB
Volume: 104
Category: Article
ISSN: 1096-7192
DOI: 10.1016/j.ymgme.2011.05.004

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