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Neurology|July 4, 2007
Clinical and neuropathologic study of a French family with a mutation in the neuroserpin geneI Gourfinkel-An, C Duyckaerts, A Camuzat, et al.Genomics|April 18, 1998
Genomic organization of the human SPOCK gene and its chromosomal localization to 5q31F Charbonnier, J P Périn, M G Mattei, et al.The Journal of Biological Chemistry|February 23, 1996
Structure and cellular distribution of mouse brain testican. Association with the postsynaptic area of hippocampus pyramidal cellsF Bonnet, J P Périn, F Charbonnier, et al.Human Genetics|June 1, 1996
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13A Camuzat, J M Rozet, H Dollfus, et al.Archives of Neurology|March 14, 2000
Frequency of the DYT1 mutation in primary torsion dystonia without family historyD Brassat, A Camuzat, M Vidailhet, et al.American Journal of Human Genetics|February 1, 1995
A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13S Gerber, J M Rozet, D Bonneau, et al.Human Molecular Genetics|August 1, 1995
A gene for Leber's congenital amaurosis maps to chromosome 17pA Camuzat, H Dollfus, J M Rozet, et al.American Journal of Human Genetics|May 23, 2000
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardationA Herman-Bert, G Stevanin, J C Netter, et al.Neurology|June 15, 2007
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?P Charles, A Camuzat, N Benammar, et al.Brain : a Journal of Neurology|September 26, 2001
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxiaH Fujigasaki, J J Martin, P P De Deyn, et al.Pageof 2