The Clinical and Audiologic Features of Hearing Loss Due to Mitochondrial Mutations

Mitochondrial tRNA mutations associated with deafness

(2012) Jing Zheng et al.   MITOCHONDRION

The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population

(2011) Megan Ealy et al.   LARYNGOSCOPE

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

(2010) Jianxin Lu et al.   MITOCHONDRION

Screening of the General Polish Population for Deafness-Associated Mutations in Mitochondrial 12S rRNA and tRNASer(UCN) Genes

(2009) Małgorzata Rydzanicz et al.   Genetic Testing and Molecular Biomarkers

Prevalence of Mitochondrial 1555A→G Mutation in European Children

(2009) Maria Bitner-Glindzicz et al.   NEW ENGLAND JOURNAL OF MEDICINE

GJB2,SLC26A4and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects

(2008) Yu-Fen Guo et al.   ACTA OTO-LARYNGOLOGICA

Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature

(2008) Stefano Berrettini et al.   BIOSCIENCE REPORTS

Genetics of aminoglycocide-induced and prelingual non-syndromic mitochondrial hearing impairment: A review

(2008) L. Hema Bindu et al.   INTERNATIONAL JOURNAL OF AUDIOLOGY

Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients

(2008) Annelies Konings et al.   MITOCHONDRION