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Spastic paraplegia 35
- ... classified as having a separate disorder called spastic paraplegia 35. People with mutations in this gene resulting in ... condition. Dysmyelinating leukodystrophy and spastic paraparesis FAHN Spastic paraplegia 35 Genetic Testing Registry: Hereditary spastic paraplegia 35 Fatty ...
- ... classified as having a separate disorder called spastic paraplegia 35. People with mutations in this gene resulting in ... hydroxylase domain containing 1 FAXDC1 FLJ25287 SCS7 spastic paraplegia 35 (autosomal recessive) SPG35 Tests of FA2H PubMed FATTY ...
- ... Central Blackstone C. Cellular pathways of hereditary spastic paraplegia. Annu Rev Neurosci. 2012;35:25-47. doi: 10.1146/annurev-neuro-062111- ...
- ... of myelination and atrophy on cerebral imaging in 35 patients with PLP1-related disorders. Dev Med Child ...
- ... deoxyguanosine to another molecule called guanine. More than 35 PNP gene mutations have been identified in individuals ... nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections. J Child Neurol. 2007 Jun; ...