Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31

Ítems similars

• REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31
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• Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31
  per: Züchner, Stephan, et al.
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• Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families
  per: Ma, Xinran, et al.
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• REEPing the benefits of an animal model of hereditary spastic paraplegia
  per: Deutch, Ariel Y., et al.
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• Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
  per: Schlang, Katharina J, et al.
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