FIGURE 5
FROM:
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
BACK TO ARTICLEFigure 5.
Genomic sequence of part of exon 23, intron 23 and exon 24, including the splice-site mutation c.IVS23+2321T>G (arrow). The boxed sequence is the coding region of exons 23 and 24. The nucleotides indicated in bold are the cryptic splice sites and the underlined sequence is the cryptic exon itself.
