Postlingual Hearing Loss as a Mitochondrial 3243A>G Mutation Phenotype

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

(2011) Małgorzata Rydzanicz et al.   MOLECULAR GENETICS AND METABOLISM

Clinical spectrum of the MELAS mutation in a large pedigree

(2010) M.S. Damian et al.   ACTA NEUROLOGICA SCANDINAVICA

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

Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss

(2010) Tomofumi Kato et al.   JOURNAL OF HUMAN GENETICS

Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity

(2010) Min-Xin Guan   MITOCHONDRION

URINE HETEROPLASMY IS THE BEST PREDICTOR OF CLINICAL OUTCOME IN THE m.3243A>G mtDNA MUTATION

(2009) R. G. Whittaker et al.   NEUROLOGY

Pathogenic Mitochondrial DNA Mutations Are Common in the General Population

(2008) Hannah R. Elliott et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Macular Dystrophy Associated With the A3243G Mitochondrial DNA Mutation

(2008) Michel Michaelides   ARCHIVES OF OPHTHALMOLOGY