European Journal of Human Genetics - Figure 1 for article: A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss

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A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss

Nele Hilgert, Vedat Topsakal, Joost van Dinther, Erwin Offeciers, Paul Van de Heyning and Guy Van Camp

Figure 1.

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Pedigree of the Belgian family 1 with non-syndromic autosomal dominant hearing loss. The haplotypes are shown below each symbol, with the linked haplotype indicated by a box. Black symbols indicate affected individuals, open symbols represent unaffected individuals and question marks indicate individuals with an uncertain diagnosis. The analyzed markers are listed from centromere (top) to telomere (bottom).

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FIGURE 1

A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss

Figure 1.