共 50 条
- [1] A novel de novo disease-causing variant in ATL1 in a pediatric patient with spastic paraplegia NEUROLOGY AND CLINICAL NEUROSCIENCE, 2025, 13 (02): : 159 - 161
- [2] Exome sequencing shows a novel de novo mutation in ATL1 NEUROLOGY AND CLINICAL NEUROSCIENCE, 2014, 2 (01): : 1 - 4
- [3] Myoclonus-Dystonia plus Syndrome in a Patient Carrying a Novel TCF20 Variant MOVEMENT DISORDERS CLINICAL PRACTICE, 2025, 12 (01): : 105 - 107
- [4] Novel mutation in the ATL1 with autosomal dominant hereditary spastic paraplegia presented as dysautonomia AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL, 2014, 185 : 141 - 143
- [7] Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia Russian Journal of Genetics, 2022, 58 : 1145 - 1153