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©The Author(s) 2022.
World J Clin Cases. Jan 14, 2022; 10(2): 703-708
Published online Jan 14, 2022. doi: 10.12998/wjcc.v10.i2.703
Published online Jan 14, 2022. doi: 10.12998/wjcc.v10.i2.703
Figure 4 Conservation of amino acids in the context of the frameshift mutation.
Amino acid sequence alignments of some of the amino acids affected by the mutation are shown for selected species. The red rectangle highlights the first amino acid affected by the frameshift mutation. This novel mutation is located in a relatively conserved domain.
- Citation: Huang X, Fan DS. Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation: A case report. World J Clin Cases 2022; 10(2): 703-708
- URL: https://www.wjgnet.com/2307-8960/full/v10/i2/703.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i2.703