A recent study published in PubMed details the clinical features of four unrelated Japanese patients diagnosed with autosomal recessive spinocerebellar ataxia type 32. This research contributes to the understanding of the disease's presentation and may inform future studies.
clinical features of four unrelated japanese patients with autosomal recessive spinocerebellar ataxia type 32
Original title: “Clinical features of four unrelated Japanese patients with autosomal recessive spinocerebellar ataxia type 32.”