Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Physician Scientist Award (K11)
Project #
5K11HD000940-05
Application #
2194409
Study Section
Mental Retardation Research Committee (HDMR)
Project Start
1991-07-01
Project End
1997-06-30
Budget Start
1995-07-01
Budget End
1997-06-30
Support Year
5
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Utah
Department
Neurology
Type
Schools of Medicine
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
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Flanigan, K; Gardner, K; Alderson, K et al. (1996) Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1. Am J Hum Genet 59:392-9
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Fouad, G T; Servidei, S; Durcan, S et al. (1996) A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q. Am J Hum Genet 59:135-9
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Ptacek, L J; Tawil, R; Griggs, R C et al. (1994) Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 77:863-8
Gouw, L G; Digre, K B; Harris, C P et al. (1994) Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred. Neurology 44:1441-7
Ptacek, L J; Tawil, R; Griggs, R C et al. (1994) Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. Neurology 44:1500-3

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