Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference27 articles.
1. X-Linked Pure Familial Spastic Paraparesis
2. Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia
3. Novel syndromic form of X-linked complicated spastic paraplegia
4. X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype
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1. Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview;Frontiers in Molecular Biosciences;2021-11-26
2. Proteolipid protein–deficient myelin promotes axonal mitochondrial dysfunction via altered metabolic coupling;Journal of Cell Biology;2016-11-21
3. Neuromuscular disorders: genes, genetic counseling and therapeutic trials;Genetics and Molecular Biology;2016-09
4. Clinical features and management of hereditary spastic paraplegia;Arquivos de Neuro-Psiquiatria;2014-03
5. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance;Journal of the Neurological Sciences;2012-07
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