QuickView for AFG3L2 (gene)

1. Multifaceted Roles of AFG3L2, a Mitochondrial ATPase in Relation to Neurological Disorders.
2. Optic Neuropathy AFG3L2 Related in a Patient Affected by Congenital Stationary Night Blindness.
3. Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through m…
4. AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian Patients.
5. Astrocyte-specific deletion of the mitochondrial m-AAA protease reveals glial contribution to neurod…

There were no clinical trials for AFG3L2