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. 2010 May 11;133(6):1798–1809. doi: 10.1093/brain/awq109

Figure 1.

Figure 1

Location of mutations in the different domains of TRPV4 protein. Neuropathy causing mutations are indicated as well as previously described mutations for autosomal-dominant brachyolmia, spondylometaphyseal dysplasia (SMDK), Kozlowski type and metatropic dysplasia. Mutations identified in this study are in bold. The new neuropathy associated mutations are indicated by asterisks.