J Mov Disord.
2025 Apr;18(2):185-189. 10.14802/jmd.24259.
Spastic Paraplegia 82 in Two Asian Indian Siblings With PCYT2 Mutations
- Affiliations
-
- 1Department of Neurology, All India Institute of Medical Sciences, New Delhi, India
- 2Department of Neuroimaging and Interventional radiology, All India Institute of Medical Sciences, New Delhi, India
- KMID: 2567167
- DOI: http://doi.org/10.14802/jmd.24259
- Full Text Links
-
- Actions
-
Cited
- CITED
-
- Close
- Share
-
- Similar articles
-
- Hereditary spastic paraplegia with thin corpus callosum due to novel homozygous mutation in SPG11 gene
- Two novel mutations in ALDH18A1 and SPG11 gene found by whole-exome sequencing in spastic paraplegia disease patients in Iran
- Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11
- Hereditary Spastic Paraplegia
- Pure or Complex Hereditary Spastic Paraplegia Type 4?
