Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families

2024-11-09201810.1212/NXG.00000000000002182-s2.0-85048716971https://hdl.handle.net/20.500.14288/241pdfClinical neurologyHomozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 familiesJournal Article2376-7839https://doi.org/10.1212/NXG.0000000000000218430501700010N/ANOIR01429