QuickView for AFG3L2;jsessionid=608814BCC0483F7174DB28C456EECBE1 (gene)

1. Astrocyte-specific deletion of the mitochondrial m-AAA protease reveals glial contribution to neurod…
2. Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia.
3. Netrin-1 attenuates cerebral ischemia/reperfusion injury by limiting mitochondrial ROS and Ca2+ leve…
4. Molecular insights into the m-AAA protease-mediated dislocation of transmembrane helices in the mito…
5. AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival.

There were no clinical trials for AFG3L2;jsessionid=608814BCC0483F7174DB28C456EECBE1