Genetics Research International / 2011 / Article / Fig 1

Research Article

Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene

Figure 1

Pedigree drawing and haplotype of family 4208 with the genetic interval on chromosome 11. Filled symbols denote individuals with ARNSHI, while clear symbols represent hearing individuals. The haplotype segregating with ARNSHI is shown in a box and includes short tandem repeat markers and the RDX deletion c.1076_1079delTTAA (p.Ile359Lysfs*6) as a triangle. The positions of the TECTA and RDX genes relative to the genome scan markers are labelled. The genetic interval with genotyped marker loci and locations of RDX and TECTA genes were indicated on the cartoon of chromosome 11.

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.