Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).

Prasad, S

Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA). [electronic resource] - Human mutation Dec 2000 - 502-8 p. digital

Publication Type: Journal Article

1098-1004

10.1002/1098-1004(200012)16:6<502::AID-HUMU7>3.0.CO;2-4 doi


Alleles
Amino Acid Substitution--genetics
Arginine--genetics
Connexin 26
Connexins--blood
Cysteine--genetics
Deafness--congenital
Genetic Testing--methods
Genetic Variation
Hearing Loss, Sensorineural--congenital
Humans
Mutation--genetics
Sequence Deletion--genetics