Publication | Open Access

Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia

Autosomal-recessive Cerebellar AtaxiaMendelian DisorderNeurogenomicsGenetic DisorderNext-generation SequencingGeneticsDegenerative DiseaseNeurologyDisease Gene IdentificationMedicine