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 requiring aminoglycosides?

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Mitochondrial hearing loss mutations among Finnish preterm and term-born infants.

P2860

Q47114347-53B99A23-53BC-4CC0-930A-FA33C517E84D

P2860

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 requiring aminoglycosides?

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2015 nî lūn-bûn

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2015年論文

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2015年論文

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2015年論文

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A meta-analysis and systematic ...... tes requiring aminoglycosides?

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A meta-analysis and systematic ...... tes requiring aminoglycosides?

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A meta-analysis and systematic ...... tes requiring aminoglycosides?

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A meta-analysis and systematic ...... tes requiring aminoglycosides?

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A meta-analysis and systematic ...... tes requiring aminoglycosides?

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A meta-analysis and systematic ...... tes requiring aminoglycosides?

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P1476

A meta-analysis and systematic ...... tes requiring aminoglycosides?

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P2093

Brian D Westerberg

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Sanjiv K Bhimrao

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Titus S Ibekwe

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P275

Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported

P2860

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Ototoxicity of amikacin

Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.

Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss.

Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.

Mitochondrial deafness mutations reviewed.

Aminoglycoside antibiotics.

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

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

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105-113

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scholarly article

review article

meta-analysis

P356

10.4103/0189-6725.160342

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English

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F Kozak

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2015-04-01T00:00:00Z

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26168747

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Angliavandeniai

preventive health services

biomedical investigative technique

Achyolli

RNA analysis

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4955414

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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 requiring aminoglycosides?

about

P2860

P2860

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 requiring aminoglycosides?

description

name

type

label

prefLabel

P1433

P1476

P2093

P275

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P275

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932