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Rydning, S. et al. (2018). A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia. European journal of neurology. pp. 943-e71. [Online].
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Rydning, S. et al. (2018). A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia. European journal of neurology. pp. 943-e71. [Online].