Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.

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Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway

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Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.

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Genome-wide association analys ...... for hearing function and loss.

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Genome-wide association analys ...... for hearing function and loss.

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Genome-wide association analys ...... for hearing function and loss.

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Genome-wide association analys ...... for hearing function and loss.

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Adrian Davis

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Aileen Bahl

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Anna Morgan

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David P Corey

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Deborah I Scheffer

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Lisa Nolan

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Mariateresa Di Stazio

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Mario Pirastu

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5655-5664

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scholarly article

meta-analysis

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10.1093/HMG/DDV279

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26188009

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genome-wide association study

RNA-Seq

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4572074

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Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.

about

P2860

P2860

Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.

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