Associated Papers
A Single-cell Transcriptome-wide Association Study Reveals Susceptibility Genes for Age-related Hearing Loss.
Li Y et al.
Genomics, Proteomics & Bioinformatics, 2026
Functional and Biochemical Consequences of Disease Variants in Neurotransmitter Transporters: A Special Emphasis on Folding and Trafficking Deficits.
Bhat S et al.
Pharmacology & Therapeutics, 2021
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.
Ma Z et al.
Human Molecular Genetics, 2017
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