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Publications by Fuyuki Miya

Variants Encoding a Restricted Carboxy-Terminal Domain of SLC12A2 Cause Hereditary Hearing Loss in Humans

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2020English

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Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss

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Loss-Of-Function Variants in Endothelial Lipase Are a Cause of Elevated HDL Cholesterol in Humans

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Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population

Journal of Human Genetics
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2015English

Hereditary Bilateral Sudden Sensorineural Hearing Loss

Bratislava Medical Journal
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Genotype-Phenotype Correlation in Hereditary Hearing Loss

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Gene Therapy for Hereditary Hearing Loss

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Congenital Cytomegalovirus Infection: A Cause of Sensorineural Hearing Loss.

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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

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Labyrinthine Window Rupture as a Cause of Acute Sensorineural Hearing Loss

European Archives of Oto-Rhino-Laryngology
MedicineOtorhinolaryngology
2011English

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