Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss

Novel human mitochondrial tRNAphemutation in a patient with hearing impairment: A case study

(2012) Mohammad Ali Dowlati et al.   Mitochondrial DNA

Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation

(2011) Hideki Mutai et al.   BMC Medical Genetics

Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition

(2011) A Sudo et al.   JOURNAL OF LARYNGOLOGY AND OTOLOGY

The search of a genetic basis for noise-induced hearing loss (NIHL)

(2010) Ronaldo Serafim Abreu-Silva et al.   ANNALS OF HUMAN BIOLOGY

Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss

(2010) Małgorzata Rydzanicz et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

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

(2010) Jianxin Lu et al.   MITOCHONDRION

Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness

(2010) Melissa de Freitas Cordeiro-Silva et al.   MOLECULAR BIOLOGY REPORTS

Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment

(2009) Vanessa Cristine Sousa de Moraes et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

(2009) Jianxin Lu et al.   MITOCHONDRION

Expression and Maintenance of Mitochondrial DNA

(2008) Gerald S. Shadel   AMERICAN JOURNAL OF PATHOLOGY

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