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
Structure analyses reveal a regulated oligomerization mechanism of the PlexinD1/GIPC/myosin VI complex.
Shang G et al.
Elife, 2017
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.
Ammar-Khodja F et al.
Molecular Genetics & Genomic Medicine, 2015
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