gms | German Medical Science


Figure 3:. Genes cloned for non syndromic autosomal dominant and autosomal recessive hearing disorders. Mutations in some of these genes (*) can also cause syndromic hearing impairment: Ush1B, DFNB2 and DFNA11: MYO7A; DFNB12 and Ush1D: CDH23; DFNB18 and Ush1C: USH1C; DFNB23 and Ush1F: PCDH15, DFNB4 and Pendred syndrome: SLC26A4; DFNA6/14 and Wolfram syndrome: WFS1; DFNA13 and Stickler syndrome type 2: COL11A2.