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Figure 2 | BMC Medical Genetics

Figure 2

From: Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Figure 2

MYO15A gene structure and a 3D model of the MyTH4 domain. (A) The novel MYO15A mutations reported in this study are indicated at the top of the figure, and previously reported mutations are listed at the bottom of the figure. (B) The MyTH4 domain comprises an alpha-helix (red) and loops (green). The locations of R2146 and S2161 are shown in magenta and cyan, respectively.

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