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Publications While At HealthPartners

selected publications

Journal Article

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12. 

Neurogenetics. 2006

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. 

American Journal of Human Genetics. 2006

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations. 

Neurogenetics. 2004

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full name

P. C. Gaskell

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