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Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2001
CYP2D6 polymorphism in Parkinson's disease: the Rotterdam StudyB S Harhangi, B A Oostra, P Heutink, et al.
Human Molecular Genetics|April 21, 2009
Ectopic expression of CGG containing mRNA is neurotoxic in mammalsVera Hashem, Jocelyn N Galloway, Mayra Mori, et al.
Development Genes and Evolution|April 9, 2005
Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 geneSandra van 't Padje, Bart Engels, Lau Blonden, et al.
Biological Psychiatry|January 3, 2009
The GAB2 gene and the risk of Alzheimer's disease: replication and meta-analysisM Arfan Ikram, Fan Liu, Ben A Oostra, et al.
Genomics|August 1, 1991
Laser microdissection of the fragile X region: identification of cosmid clones and of conserved sequences in this regionM Djabali, C Nguyen, I Biunno, et al.
The EMBO Journal|June 1, 1988
Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complexL H Hoefsloot, M Hoogeveen-Westerveld, M A Kroos, et al.
The New England Journal of Medicine|December 26, 1996
A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infectionM J Newport, C M Huxley, S Huston, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2005
Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndromeLeonardo Restivo, Francesca Ferrari, Enrica Passino, et al.
Biochemical and Biophysical Research Communications|September 16, 1991
Identification of a point mutation in the human lysosomal alpha-glucosidase gene causing infantile glycogenosis type IIM M Hermans, E de Graaff, M A Kroos, et al.
The Journal of Physiology|December 24, 2008
Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout miceYair Pilpel, Aleksander Kolleker, Sven Berberich, et al.
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