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US07811762B2 Identification of a novel gene underlying familial spastic paraplegia 有权
鉴定家族性痉挛性截瘫的新基因

Identification of a novel gene underlying familial spastic paraplegia
Abstract:
Methods of identifying polymorphisms associated with hereditary spastic paraplegia (SPG), are described. The polymorphisms associated with SPG include specific mutations in the receptor expression enhancing protein 1 (REEP1) gene. Also described are methods of diagnosis of SPG.
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