Associated Papers
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
Functional proteomics, human genetics and cancer biology of GIPC family members.
Katoh M
Experimental & Molecular Medicine, 2013
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
Rehman AU et al.
Human Genetics, 2011
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