Clinical Application of Screening for GJB2 Mutations before Cochlear Implantation in a Heterogeneous Population with High Rate of Autosomal Recessive Nonsyndromic Hearing Loss

Table 1

GJB2 genotypes in patients carrying no 35delG mutations. Homozygote mutations are marked with an asterisk.

Genotype	Frequency	Percent
V1531	4	25%
R184P*	2	12.5%
167DelT*	2	12.5%
V27I SNP*	2	12.5%
G130V	1	6.3%
235delC/R184P	1	6.3%
R127H	1	6.3%
SNP N26N*	1	6.3%
R32C*	1	6.3%
R151P*	1	6.3%
Total	16	100%