Exome sequencing coupled with homozygosity mapping was used to identify a transition mutation (c.794T>C; p.Leu265Ser) in ELMOD3 at the DFNB88 locus that is associated with nonsyndromic deafness in a l
Derived allele frequencies for each population sample at each variable site for which there was a high-quality genotype call for all 31 individuals, and the outgroup species were fixed for the ancestr
