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presbycusis
(phenotype)
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Genetic Markers
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Most Correlated SNPs
No genes found
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Pathway Enrichment
Most Correlated Biogroups
STARK_PREFRONTAL_CORTEX_22Q11_DELETION_DN
SWEET_LUNG_CANCER_KRAS_UP
KIM_ALL_DISORDERS_OLIGODENDROCYTE_NUMBER_CORR_UP
MODULE_114
PILON_KLF1_TARGETS_DN
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Most Correlated Studies
Inferior colliculus tissue from presbycusic middle-aged mice
Novel approach to select genes using functional hearing
Cochlear tissues from CMAH knockout mice
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Literature
Most Relevant Literature
A Novel Therapy for Presbycusis.
Correlation between mitochondrial DNA 4977 bp deletion and presbycusis: A system review and meta-ana…
Age-related Activation of Cyclic GMP-AMP synthase-Stimulator of Interferon Genes Signaling in the Au…
Can prestin level be a biomarker for determining sensorineural hearing loss?
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness u…
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Most Relevant Clinical Trials
Mitochondrial Genetics of Presbycusis
Postural Modification and Hearing Aids in Presbycusis
Study of the Association Between Presbycusis With the Incidence of Frailty
Efficacy and Safety of Liuwei Dihuang Pill Versus Placebo in Presbycusis With Shen (Kidney)-Yin Defi…
Effects of Huperzine A on Presbycusis(Δ,kHz, dB,MMSE, AD)
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