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Mitochondrial mutations associated with aminoglycoside ototoxicity and hearing loss susceptibility identified by meta-analysis
W **g, H Zongjie, F Denggang, H Na, Z Bin… - Journal of medical …, 2015 - jmg.bmj.com
Background Genetic variations, including mitochondrial mutations, are important
contributors to hearing loss, especially in children, and newborn genetic screens for hearing …
contributors to hearing loss, especially in children, and newborn genetic screens for hearing …
Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia)
VY Danilchenko, MV Zytsar, EA Maslova… - Diagnostics, 2021 - mdpi.com
Hereditary hearing loss (HL) is known to be highly locus/allelic heterogeneous, and the
prevalence of different HL forms significantly varies among populations worldwide …
prevalence of different HL forms significantly varies among populations worldwide …
Genetic etiology of hearing loss in Russia
OL Posukh - Human Genetics, 2022 - Springer
Prevalence and locus/allelic heterogeneity of the hereditary hearing loss (HL) vary
significantly in different human populations. Investigation of the hereditary HL diversity and …
significantly in different human populations. Investigation of the hereditary HL diversity and …
Association between cardiovascular health and hearing function: Pure-tone and distortion product otoacoustic emission measures
KM Hutchinson, H Alessio, RR Baiduc - 2010 - pubs.asha.org
Purpose A reduction in hearing sensitivity is often considered to be a normal age-related
change. Recent studies have revisited prior ways of thinking about sensory changes over …
change. Recent studies have revisited prior ways of thinking about sensory changes over …
High prevalence of m. 1555A> G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect
TV Borisova, AM Cherdonova, VG Pshennikova… - Scientific Reports, 2024 - nature.com
Abstract Mitochondrial forms account approximately 1–2% of all nonsyndromic cases of
hearing loss (HL). One of the most common causative variants of mtDNA is the m. 1555A> G …
hearing loss (HL). One of the most common causative variants of mtDNA is the m. 1555A> G …
Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation
Y Zhu, S Huang, D Kang, M Han, G Wang, Y Yuan… - BMC genetics, 2014 - Springer
Background Mitochondrial cytopathies are characterized by a large variability of clinical
phenotypes and severity. The amount of mutant mitochondrial DNA (mtDNA) in a cell, called …
phenotypes and severity. The amount of mutant mitochondrial DNA (mtDNA) in a cell, called …
Haplotype diversity and reconstruction of ancestral haplotype associated with the c. 35delG mutation in the GJB2 (Cx26) gene among the Volgo-Ural populations of …
LU Dzhemileva, OL Posukh, NA Barashkov… - Acta Naturae …, 2011 - cyberleninka.ru
The mutations in the GJB2 (Сх26) gene make the biggest contribution to hereditary hearing
loss. The spectrum and prevalence of the GJB2 gene mutations are specific to populations …
loss. The spectrum and prevalence of the GJB2 gene mutations are specific to populations …
Utility of genetic testing for the detection of late-onset hearing loss in neonates
BG Lim, RH Clark, AS Kelleher, Z Lin, AR Spitzer - 2013 - pubs.asha.org
Purpose The purpose of this study was to demonstrate the utility of molecular testing in the
detection of potentially important causes of delayed hearing loss missed by current …
detection of potentially important causes of delayed hearing loss missed by current …
Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c. 35delG mutations in a family with hearing loss
H Kokotas, M Grigoriadou, L Yang, M Lodahl… - International Journal of …, 2011 - Elsevier
OBJECTIVE: Mitochondrial mutations have been shown to be responsible for syndromic as
well as non-syndromic hearing loss. The G7444A mitochondrial DNA mutation affects …
well as non-syndromic hearing loss. The G7444A mitochondrial DNA mutation affects …
A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates …
TS Ibekwe, SK Bhimrao, BD Westerberg… - African Journal of …, 2015 - journals.lww.com
Background: This was a meta-analysis and systematic review to determine the global
prevalence of the mitochondrially encoded 12S RNA (MT-RNR1) genetic mutation in order …
prevalence of the mitochondrially encoded 12S RNA (MT-RNR1) genetic mutation in order …