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Publications by Wenhui Lin

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

Molecular Medicine Reports

English

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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

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Cardiovascular Medicine

Cardiology

2017

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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

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Novel Homozygous PANK2 Mutation Identified in a Consanguineous Chinese Pedigree With Pantothenate Kinase-Associated Neurodegeneration

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Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation

AUDIOLOGY JAPAN

2003

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Characterization of the Kyoto Circling (KCI) Rat Carrying a Spontaneous Nonsense Mutation in the Protocadherin 15 (Pcdh15) Gene

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A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree

Molecular genetics & genomic medicine

Genetics

Molecular Biology

2020

English

A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree

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Characterization of a Tumor-Associated Activating Mutation of the P110β PI 3-Kinase

PLoS ONE

Multidisciplinary

2013

English

A Novel BMPR2 Mutation Associated With Pulmonary Arterial Hypertension in an Octogenarian

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Wenhui Lin

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

Related publications

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

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

Novel Homozygous PANK2 Mutation Identified in a Consanguineous Chinese Pedigree With Pantothenate Kinase-Associated Neurodegeneration

Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation

Characterization of the Kyoto Circling (KCI) Rat Carrying a Spontaneous Nonsense Mutation in the Protocadherin 15 (Pcdh15) Gene

A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree

A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree

Characterization of a Tumor-Associated Activating Mutation of the P110β PI 3-Kinase

A Novel BMPR2 Mutation Associated With Pulmonary Arterial Hypertension in an Octogenarian