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Publications by Asami Tsushima
Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Hearing Loss Is Associated With the 12S rRNA C1494T Mutation in Three Han Chinese Pedigrees
Gene
Medicine
Genetics
Related publications
Maternally Inherited Deafness Associated With a T1095C Mutation in the mDNA
European Journal of Human Genetics
Genetics
Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Noncoding Mutations of HGF Are Associated With Nonsyndromic Hearing Loss, DFNB39
American Journal of Human Genetics
Genetics
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
Biochemistry
Cell Biology
Molecular Biology
Biophysics
SOD2 V16A SNP in the Mitochondrial Targeting Sequence Is Associated With Noise Induced Hearing Loss in Chinese Workers
Disease Markers
Biochemistry
Medicine
Clinical Biochemistry
Molecular Biology
Genetics
Mitochondrial COI/tRNASer(UCN) G7444A Mutation May Be Associated With Aminoglycoside-Induced and Non-Syndromic Hearing Impairment
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation
AUDIOLOGY JAPAN
The R245X Mutation of PCDH15 in Ashkenazi Jewish Children Diagnosed With Nonsyndromic Hearing Loss Foreshadows Retinitis Pigmentosa
Pediatric Research
Child Health
Pediatrics
Perinatology
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
