QuickView for SCA28 (gene)

1. Multifaceted Roles of AFG3L2, a Mitochondrial ATPase in Relation to Neurological Disorders.
2. AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian Patients.
3. AFG3L2 and ACO2-Linked Dominant Optic Atrophy: Genotype-Phenotype Characterization Compared to OPA1 …
4. Astrocyte-specific deletion of the mitochondrial m-AAA protease reveals glial contribution to neurod…
5. Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia.

There were no clinical trials for SCA28