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Publications by Feilong Meng

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

Journal of Biological Chemistry

English

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

English

Related publications

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

Biochemical and Biophysical Research Communications

English

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

Internal Medicine

Medicine

2017

English

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

European Journal of Human Genetics

Genetics

2003

English

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

Molecular Medicine Reports

English

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

Internal Medicine

Medicine

2019

English

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

Indonesian Journal of Agricultural Science

2016

English

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

Indonesian Journal of Agricultural Science

2016

English

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

Journal of Investigative Dermatology

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Feilong Meng

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

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

Related publications

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

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