Phenotypic Variability in ATP13A2 Mutations: The First Report of SPG78 From India
- PMID: 40583806
- PMCID: PMC12580734
- DOI: 10.14802/jmd.25100
Phenotypic Variability in ATP13A2 Mutations: The First Report of SPG78 From India
Conflict of interest statement
The authors have no financial conflicts of interest.
References
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- Shribman S, Reid E, Crosby AH, Houlden H, Warner TT. Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches. Lancet Neurol. 2019;18:1136–1146. - PubMed
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