Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
- PMID: 25352184
- PMCID: PMC4453490
- DOI: 10.1136/jnnp-2014-308625
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
Keywords: GENETICS; HEREDIT SPASTIC PARAPLEGIA; NEUROGENETICS.
References
-
- Lo Giudice T, Lombardi F, Santorelli FM, et al. Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms. Exp Neurol 2014;261C:518–39. - PubMed
-
- Schüle R, Holland-Letz T, Klimpe S. The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity. Neurology 2006;67:430–4. - PubMed
-
- Carlesimo GA, Caltagirone C, Gainotti G. The mental deterioration battery: normative data, diagnostic reliability and qualitative analyses of cognitive impairment. The group for the standardization of the mental deterioration battery. Eur Neurol 1996;36:378–84. - PubMed
-
- Meissner MH, Gloviczki P, Bergan J, et al. Primary chronic venous disorders. J Vasc Surg 2007;46:54S–67S. - PubMed
-
- Hindocha S, John S, Stanley JK, et al. The heritability of Dupuytren's disease: familial aggregation and its clinical significance. J Hand Surg Am 2006;31:204–10. - PubMed
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