(PDF) Contribution of the tRNAIle4317A>G Mutation to the

Contribution of the tRNAIle4317A>G Mutation to the Phenotypic Manifestation of the Deafness-Associated Mitochondrial 12S rRNA 1555A>G Mutation

Journal of Biological Chemistry - United States

doi 10.1074/jbc.ra117.000530

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January 18, 2018

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American Society for Biochemistry & Molecular Biology (ASBMB)

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Amanote Research

Contribution of the tRNAIle4317A>G Mutation to the Phenotypic Manifestation of the Deafness-Associated Mitochondrial 12S rRNA 1555A>G Mutation

Journal of Biological Chemistry - United States

doi 10.1074/jbc.ra117.000530

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

The ND4 G11696A Mutation May Influence the Phenotypic Manifestation of the Deafness-Associated 12S rRNA A1555G Mutation in a Four-Generation Chinese Family

Authors' Reply to 'Heteroplasmy of the M.3243A>G Mutation May Influence Phenotypic Heterogeneity'

Lack of a Modulative Factor in Locus 8p23 in a Finnish Family With Nonsyndromic Sensorineural Hearing Loss Associated With the 1555A>G Mitochondrial DNA Mutation

The Mitochondrial Transfer RNAAsp A7551G Mutation May Contribute to the Clinical Expression of Deafness Associated With the A1555G Mutation in a Pedigree With Hearing Impairment

Phenotypic Diversity of Myoclonus Epilepsy Associated With Ragged-Red Fibers With an 8344A>G mtDNA Mutation

Contribution to the Phylogeny of the Pangasiidae Based on Mitochondrial 12s Rdna

Contribution to the Phylogeny of the Pangasiidae Based on Mitochondrial 12s Rdna

Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family

GNA11 Mutation as a Cause of Sturge Weber Syndrome - Expansion of the Phenotypic Spectrum of G-Protein Related Mosaicism and the Associated Clinical Diagnoses

Amanote Research

Contribution of the tRNAIle4317A>G Mutation to the Phenotypic Manifestation of the Deafness-Associated Mitochondrial 12S rRNA 1555A>G Mutation

Journal of Biological Chemistry - United States

doi 10.1074/jbc.ra117.000530

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

The ND4 G11696A Mutation May Influence the Phenotypic Manifestation of the Deafness-Associated 12S rRNA A1555G Mutation in a Four-Generation Chinese Family

Authors' Reply to 'Heteroplasmy of the M.3243A>G Mutation May Influence Phenotypic Heterogeneity'

Lack of a Modulative Factor in Locus 8p23 in a Finnish Family With Nonsyndromic Sensorineural Hearing Loss Associated With the 1555A>G Mitochondrial DNA Mutation

The Mitochondrial Transfer RNAAsp A7551G Mutation May Contribute to the Clinical Expression of Deafness Associated With the A1555G Mutation in a Pedigree With Hearing Impairment

Phenotypic Diversity of Myoclonus Epilepsy Associated With Ragged-Red Fibers With an 8344A>G mtDNA Mutation

Contribution to the Phylogeny of the Pangasiidae Based on Mitochondrial 12s Rdna

Contribution to the Phylogeny of the Pangasiidae Based on Mitochondrial 12s Rdna

Obesity Associated With a Novel Mitochondrial tRNACys 5802A&gt;G Mutation in a Chinese Family

GNA11 Mutation as a Cause of Sturge Weber Syndrome - Expansion of the Phenotypic Spectrum of G-Protein Related Mosaicism and the Associated Clinical Diagnoses

Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family