Sm. Leal et al., A 2ND MIDDLE-EASTERN KINDRED WITH AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING-LOSS SEGREGATES DFNB9, European journal of human genetics, 6(4), 1998, pp. 341-344
A second kindred has been identified which supports the previously rep
orted location of DFNB9. Linkage has been established to markers close
ly linked to DFNB9 which is located on 2p22-p23. The hearing impaired
individuals in this highly consanguineous kindred from Eastern Turkey
have prelingual profound hearing loss which affects all frequencies. A
genetic map of the 2p22-p23 region where DFNB9 resides was generated
using marker genotypes available from the CEPH database. All markers w
ere placed on this genetic map using a likelihood ratio criterion of 1
000:1. This map suggests that the region for DFNB9 is less than 1.08 c
M, 95% confidence interval (0-2.59 cM).