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
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.
Li YR et al.
Nature Communications, 2020
Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India.
Kalaimathi M et al.
Journal of Genetics, 2020
Structure analyses reveal a regulated oligomerization mechanism of the PlexinD1/GIPC/myosin VI complex.
Shang G et al.
Elife, 2017
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
Rehman AU et al.
Human Genetics, 2011
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human.
Charizopoulou N et al.
Nature Communications, 2011
Select a paper to view details