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  Indian J Med Microbiol
 

Figure 2: Pedigree and haplotypes (family LKO5), co-segregating nonsyndromic autosomal recessive hearing loss (filled symbols) with short tandem repeat markers at the DFNB7/11 locus. Sequence chromatogram of TMC1 gene show a novel homozygous change c.1283C>A (p.Ala428Asp) in hearing impaired children, parents and normal hearing child are heterozygous for c.1283C>A.

Figure 2: Pedigree and haplotypes (family LKO5), co-segregating nonsyndromic autosomal recessive hearing loss (filled symbols) with short tandem repeat markers at the DFNB7/11 locus. Sequence chromatogram of <i>TMC1</i> gene show a novel homozygous change c.1283C>A (p.Ala428Asp) in hearing impaired children, parents and normal hearing child are heterozygous for c.1283C>A.