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scopus: 26643408100

Krieger, E.

(Elmar Krieger)


ataxia protein patient family mutation f 145s mutation fgf 14 sequence region marker function study autosomal fgf 14 gene cerebellar brain factor model disease expansion center cerebellar ataxia chromosome tremor genet structure response member sca types fibroblast growth sca 8 locus spinocerebellar linkage family members stress locus rotterdam onset parkinsonism individual dyskinesia change level phenotype score analysis polymorphic str markers fibroblast growth factor spinocerebellar ataxia netherland novel two-point linkage analysis fgf 14 mutation protein misfolding park 7 locus examination gait ataxia parkinson acid sequence comparison pcr products fgf 14-knockout mice novel gene defect sca 8 f 145s sex-averaged linkage map atrophy dutch family fgf 14. exon 4 oxidative stress response early-onset tremor alignment report transcript 14. product finding genome defect




2 Most Recent Publications

DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism (Article)
Bonifati, V. Squitieri, F. Rizzu, P. Krieger, E. Vanacore, N. Swieten, J.C. van Brice, A. Duijn, C.M. van Meco, G. Heutink, P. Oostra, B.A.
2003-10-01
A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected] (Article)
Swieten, J.C. van Brusse, E. Heutink, P. Graaf, B.M. de Krieger, E. Graaf, R. van de Koning, I. de Maat-Kievit, A.A. Leegwater, P. Dooijes, D. Oostra, B.A.
2003-01-01