Compound heterozygous mutation of the SNX14 gene causes autosomal recessive spinocerebellar ataxia 20
Article in Frontiers in Genetics (April 2024)
The most recent citing publications are shown below. View all 3 publications that cite this research output on Dimensions.
Autosomal recessive spinocerebellar ataxia‐20 due to a novel SNX14 variant in an Indian girl
Article in American Journal of Medical Genetics Part A (February 2022)
Two Korean siblings with autosomal recessive spinocerebellar ataxia 20 caused by homozygous variants in SNX14
Article in Journal of Genetic Medicine (December 2021)