Copyright
©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 1 Pedigree of the patient’s family.
The patient’s parents and sister were all healthy. Males and females are represented as squares and circles, respectively. The patient is indicated by black-filled symbols, and unfilled symbols indicate the unaffected individuals. The mutation state is given below.
- 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