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Publications by Françoise Duriez
Whole Mitochondrial Genome Screening in Maternally Inherited Non-Syndromic Hearing Impairment Using a Microarray Resequencing Mitochondrial DNA Chip
European Journal of Human Genetics
Genetics
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Frequency of Mitochondrial Mutations in Non-Syndromic Hearing Loss as Well as Possibly Responsible Variants Found by Whole Mitochondrial Genome Screening
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Nuclear-Mitochondrial DNA Segments Resemble Paternally Inherited Mitochondrial DNA in Humans
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Mitochondrial COI/tRNASer(UCN) G7444A Mutation May Be Associated With Aminoglycoside-Induced and Non-Syndromic Hearing Impairment
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Maternally Transmitted Mitochondrial DNA Mutations Can Reduce Lifespan
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Modifier Locus for Mitochondrial DNA Disease: Linkage and Linkage Disequilibrium Mapping of a Nuclear Modifier Gene for Maternally Inherited Deafness
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Y-Linked Inheritance of Non-Syndromic Hearing Impairment in a Large Chinese Family
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DFNB1 Non-Syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
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Figure 2: Whole Genome Resequencing Analysis.
Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation
AUDIOLOGY JAPAN
