Associated Papers
Genes linked to hearing and vestibular phenotypes in humans and mice: an interspecies systematic review.
Ayoub C et al.
Human Genomics, 2025
41430327 (PubMed )
Supplement: 40246_2025_891_MOESM1_ESM.xlsx › Supplementary_Table_S2.
A review of the mechanisms underlying the role of the GIPC3 gene in hereditary deafness.
Li X et al.
Frontiers in Synaptic Neuroscience, 2022
Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population.
Petrova NV et al.
Genes, 2021
Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India.
Kalaimathi M et al.
Journal of Genetics, 2020
A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing.
Asgharzade S et al.
International Journal of Pediatric Otorhinolaryngology, 2018
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