Item Type | Name |
---|---|
Academic Article | Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. |
Academic Article | Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations. |
Concept | Muscular Atrophy, Spinal |
Concept | Atrophy |
Concept | Optic Atrophy |