Associated Papers
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?
Clabout T et al.
Genes, 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 canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family.
Siddiqi S et al.
Journal of Human Genetics, 2014
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