TY  - GEN
AU  - Prasad,S
AU  - Cucci,R A
AU  - Green,G E
AU  - Smith,R J
TI  - Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA)
SN  - 1098-1004
PY  - 2001///0111
KW  - Alleles
KW  - Amino Acid Substitution
KW  - genetics
KW  - Arginine
KW  - Connexin 26
KW  - Connexins
KW  - blood
KW  - Cysteine
KW  - Deafness
KW  - congenital
KW  - Genetic Testing
KW  - methods
KW  - Genetic Variation
KW  - Hearing Loss, Sensorineural
KW  - Humans
KW  - Mutation
KW  - Sequence Deletion
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1002/1098-1004(200012)16:6<502::AID-HUMU7>3.0.CO;2-4
ER  -