Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population

Hereditary nonsyndromic sensorineural hearing loss is a disease in which hearing loss occurs due to damage to the organ of the inner ear, the auditory nerve, or the center in the brain that is responsible for the perception of sound, characterized by wide locus and allelic heterogeneity and differen...

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Veröffentlicht in:	Genes 2021-05, Vol.12 (6), p.820
Hauptverfasser:	Petrova, Nika V, Marakhonov, Andrey V, Balinova, Natalia V, Abrukova, Anna V, Konovalov, Fedor A, Kutsev, Sergey I, Zinchenko, Rena A
Format:	Artikel
Sprache:	eng
Schlagworte:	Adaptor Proteins, Signal Transducing - genetics Adolescent Adult Auditory nerve Child Child, Preschool Congenital diseases Disease Epidemiology Families & family life Female Gene Frequency Genes Genetic disorders Genetic diversity Genotyping Hearing loss Hearing Loss, Sensorineural - genetics Heredity Humans Infant Inner ear Laboratories Male Minority & ethnic groups Mutation Mutation, Missense Parents & parenting Patients Polymorphism, Single Nucleotide Population Russia
Online-Zugang:	Volltext
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