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PMID 16826527 2006 Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.
PMID 18644145 2008 Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31).
PMID 21618648 2011 REEP1 mutations in SPG31: frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction.