(PDF) The Mitochondrial tRNAAla T5655C Mutation May

The Mitochondrial tRNAAla T5655C Mutation May Modulate the Phenotypic Expression of tRNAMet and tRNAGln A4401G Mutation in a Han Chinese Family With Essential Hypertension

International Heart Journal - Japan

doi 10.1536/ihj.16-205

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January 1, 2017

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International Heart Journal (Japanese Heart Journal)

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The Mitochondrial tRNAAla T5655C Mutation May Modulate the Phenotypic Expression of tRNAMet and tRNAGln A4401G Mutation in a Han Chinese Family With Essential Hypertension

International Heart Journal - Japan

doi 10.1536/ihj.16-205

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family

Mitochondrial tRNAAla 5601C>T Variant May Affect the Clinical Expression of the LHON‑related ND4 11778G>A Mutation in a Family

Molecular Characterization of a Pedigree Carrying the Hypertension‑associated Mitochondrial tRNAGln T4363C Mutation

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

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

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

Marked Intrafamilial Phenotypic Variation in a Family With SOD1 C111Y Mutation

Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation

Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy

Amanote Research

The Mitochondrial tRNAAla T5655C Mutation May Modulate the Phenotypic Expression of tRNAMet and tRNAGln A4401G Mutation in a Han Chinese Family With Essential Hypertension

International Heart Journal - Japan

doi 10.1536/ihj.16-205

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family

Mitochondrial tRNAAla 5601C>T Variant May Affect the Clinical Expression of the LHON‑related ND4 11778G>A Mutation in a Family

Molecular Characterization of a Pedigree Carrying the Hypertension‑associated Mitochondrial tRNAGln T4363C Mutation

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

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

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

Marked Intrafamilial Phenotypic Variation in a Family With SOD1 C111Y Mutation

Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation

Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy

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