Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. - AlzForum Alzheimer Research Paper of the Week


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Annotation

	Zhao X, Alvarado D, Rainier S, Lemons R, Hedera P, Weber CH, Tukel T, Apak M, Heiman-Patterson T, Ming L, Bui M, Fink JK. Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. Nat Genet. 2001 Nov;29(3):326-31. PubMed Abstract

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