Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry

Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss

(2015) Luciano Pereira Maniglia et al.   Brazilian Journal of Otorhinolaryngology

Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people

(2014) Yuhua Zhu et al.   ACTA OTO-LARYNGOLOGICA

Variations in mitochondrial tRNAThrgene may not be associated with coronary heart disease

(2014) Hui Pei et al.   Mitochondrial DNA

Functional Recurrent Mutations in the Human Mitochondrial Phylogeny: Dual Roles in Evolution and Disease

(2013) Liron Levin et al.   Genome Biology and Evolution

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

Searching for Digenic Inheritance in Deaf Brazilian Individuals Using the Multiplex Ligation-Dependent Probe Amplification Technique

(2011) Sueli M. da Silva-Costa et al.   Genetic Testing and Molecular Biomarkers

Role of the Mitochondrial Mutations, m.827A>G and the Novel m.7462C>T, in the Origin of Hearing Loss

(2010) Daniela Tiaki Uehara et al.   Genetic Testing and Molecular Biomarkers

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

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

Mitochondrial DNA G8363A mutation in the tRNALys gene: Clinical, biochemical and pathological study

(2009) Roberta Virgilio et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

(2008) Bobei Chen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

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

Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

(2008) Xinjian Wang et al.   Pharmacogenetics and Genomics