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UnknownTranscriptomic analysis reinforces the implication of spatacsin in neuroinflammation and neurodevelopment.
Not available
S-EPMC11743199 | biostudies-literature
UnknownIncreasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations.
Not available
S-EPMC7997841 | biostudies-literature
UnknownRAD51 haploinsufficiency causes congenital mirror movements in humans.
Not available
S-EPMC3276668 | biostudies-literature
UnknownMotor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions.
Not available
S-EPMC5839621 | biostudies-literature
UnknownClinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations.
Not available
S-EPMC11499676 | biostudies-literature
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