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Journal of Neurology, ISSN 0340-5354, 03/2019, Volume 266, Issue 3, pp. 735 - 744
SPG31 is a hereditary spastic paraplegia (HSP) caused by pathogenic variants in the REEP1 gene. The phenotype (SPG31) has occasionally been described with... 
Hereditary spastic paraplegia | REEP1 | Carpal tunnel syndrome | Polyneuropathy | Nerve conduction studies | SPG31 | DIAGNOSIS | MUTATIONS | SPECTRUM | ASSOCIATION | CLINICAL NEUROLOGY | Phenotypes | Compression | Spasticity | Nervous system | Peripheral neuropathy | Patients | Nerve conduction | Paraplegia | Autonomic nervous system | Paralysis | Spastic paraplegia | EMG
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 10/2011, Volume 32, Issue 10, pp. 1118 - 1127
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 10/2013, Volume 123, Issue 10, pp. 4134 - 4136
Journal Article
Brain Sciences, ISSN 2076-3425, 08/2018, Volume 8, Issue 8, p. 153
Hereditary spastic paraplegias (HSPs) are a group of neurodegenerative disorders characterized by weakness and spasticity of the lower extremities. HSPs are... 
Hereditary spastic paraplegias | SPG4 | SPG10 | JASPAC | SPG31 | SPG3A | MUTATION | PREVALENCE | NEUROSCIENCES | hereditary spastic paraplegias | Neurodegenerative diseases | Intellectual disabilities | Genes | Spasticity | Family medical history | Epidemiology | Consortia | Paraplegia | Molecular modelling | Gene frequency | Conflicts of interest | Ataxia | Paralysis | Mutation | Spastic paraplegia
Journal Article
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