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Gene Review

SPG19  -  spastic paraplegia 19 (autosomal dominant)

Homo sapiens

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Disease relevance of SPG19


High impact information on SPG19

  • Linkage analysis and haplotype construction permitted the identification of a novel ADPHSP locus on the long arm of chromosome 9, designated SPG19 [1].


  1. Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34. Valente, E.M., Brancati, F., Caputo, V., Bertini, E., Patrono, C., Costanti, D., Dallapiccola, B. Ann. Neurol. (2002) [Pubmed]
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