Publication | Closed Access
SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy
21
Citations
15
References
2016
Year
Novel MutationAmyotrophic Lateral SclerosisAfg3l2 Proteolytic DomainMild Cerebellar SyndromeMedicinePathologyDegenerative DiseaseNeuropathologyNeuromuscular PathologyCell Biology
| Year | Citations | |
|---|---|---|
Page 1
Page 1