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. Author manuscript; available in PMC: 2011 May 1.
Published in final edited form as: J Hum Genet. 2010 Sep 2;55(11):767–770. doi: 10.1038/jhg.2010.104

Figure 1.

Figure 1

a) Pedigree with haplotype data for family HLRB5. Solid symbols denote affected individuals. Results of genotyping are shown for two microsatellite markers. The deafness associated haplotype is shaded in gray. Alleles for each marker are denoted by letters. Allele sizes in base pairs are: D21S1252; A, 249; B, 247; C, 245; D, 239; E, 237 D21S167; A, 162; B, 154; C, 152; D,146; E, 138; F, 132.

b) Sequence trace files for the c.254 T>A mutation observed in family HLRB5 and SA18 from a normal and affected sample. The mutation is indicated by an arrow in the trace from the affected individual. The normal and mutated codons are underlined in the respective traces.