Publications by authors named "Perry C Gaskell"

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Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.
Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, Martha A Nance, Perry C Gaskell

Am J Hum Genet· August 2006

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A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12.
Stephan Züchner, Melanie E Kail, Martha A Nance, Perry C Gaskell, Ingrid K Svenson

Neurogenetics· May 2006

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A genome-wide linkage analysis of dementia in the Amish.
Daniel W Hahs, Jacob L McCauley, Amy E Crunk, Lynne L McFarland, Perry C Gaskell

Am J Med Genet B Neuropsychiatr Genet· March 2006

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A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).
Evan Reid, Mark Kloos, Allison Ashley-Koch, Lori Hughes, Simon Bevan, Perry C Gaskell

Am J Hum Genet· November 2002

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Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432.
Marcy C Speer, Felicia Lennon Graham, Erin Bonner, Keva Collier, Jeffrey M Stajich, Perry C Gaskell

Neurogenetics· October 2002

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