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

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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

15

Citations

38

References

2011

Year

Małgorzata Rydzanicz, Karolina Cywińska, Maciej Wróbel, Agnieszka Pollak, Wojciech Gawęcki, Irena Wojsyk‐Banaszak, Urszula Lechowicz, Małgorzata Mueller‐Malesińska, Monika Ołdak, Rafał Płoski,

Molecular Genetics and Metabolism

Aminoglycoside-induced Hearing LossMitochondrial FunctionPolish PatientsMitochondrial Coi/trnaserGeneticsPhysiologyAudiologyHealth SciencesMolecular BiologyGenetic DisorderAuditory PhysiologyMedicineHearing Loss

References

	Year	Citations

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