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Publications by Xiao‑Xia Ding

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

Related publications

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

Molecular Medicine Reports

English

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

Mitochondrial COI/tRNASer(UCN) G7444A Mutation May Be Associated With Aminoglycoside-Induced and Non-Syndromic Hearing Impairment

Molecular Medicine Reports

English

Prevalence of the Mitochondrial DNA A1555G Mutation in Sensorineural Deafness Patients in Island Southeast Asia

Journal of Human Genetics

Genetics

2003

English

Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation

AUDIOLOGY JAPAN

2003

English

A Novel De Novo Mutation in CEACAM16 Associated With Postlingual Hearing Impairment

Molecular Syndromology

Genetics

2015

English

Maternally Inherited Deafness Associated With a T1095C Mutation in the mDNA

European Journal of Human Genetics

Genetics

2001

English

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

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

Molecular Medicine Reports

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Xiao‑Xia Ding

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

Related publications

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

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

Mitochondrial COI/tRNASer(UCN) G7444A Mutation May Be Associated With Aminoglycoside-Induced and Non-Syndromic Hearing Impairment

Prevalence of the Mitochondrial DNA A1555G Mutation in Sensorineural Deafness Patients in Island Southeast Asia

Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation

A Novel De Novo Mutation in CEACAM16 Associated With Postlingual Hearing Impairment

Maternally Inherited Deafness Associated With a T1095C Mutation in the mDNA

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

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