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Erratum: Mutation Analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic ParaplegiaDOI 10.3988/jcn.2014.10.4.376
Mutation and clinical characteristics of autosomal-dominant hereditary spastic paraplegias in China.Semantic proximity
Three novel mutations in 20 patients with hereditary spastic paraparesis.Semantic proximity
Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia.Semantic proximity
Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients.Semantic proximity
ATL1 and REEP1 mutations in hereditary and sporadic upper motor neuron syndromes.Semantic proximity
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.Semantic proximity
Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.Semantic proximity
Genetic landscape of hereditary spastic paraplegias in the Korean population.Semantic proximity
A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegiaSemantic proximity
Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia.Semantic proximity
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3ASemantic proximity
Clinical and genetic study of a novel mutation in the REEP1 gene.Semantic proximity
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