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Journal of Molecular Neuroscience : MN|January 1, 1989
The role of mitochondrial DNA in Huntington's diseaseC C Irwin, N S Wexler, A B Young, et al.Cell|June 5, 1987
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor geneB R Seizinger, G A Rouleau, L J Ozelius, et al.Human Molecular Genetics|August 7, 2001
The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonismK Hedrich, M Kann, A J Lanthaler, et al.Annals of Neurology|November 30, 1999
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31T G Nygaard, D Raymond, C Chen, et al.Neurology|March 9, 2005
High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screeningJ Hagenah, R Saunders-Pullman, K Hedrich, et al.Human Molecular Genetics|June 9, 1998
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystoniaC Klein, M F Brin, D de Leon, et al.Annals of Neurology|July 14, 2000
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotypeC Klein, P P Pramstaller, B Kis, et al.Neurology|March 15, 2006
Phenotype-genotype correlation in Dutch patients with myoclonus-dystoniaM C F Gerrits, E M J Foncke, R de Haan, et al.Genomics|January 25, 2000
The TOR1A (DYT1) gene family and its role in early onset torsion dystoniaL J Ozelius, C E Page, C Klein, et al.Parkinsonism & Related Disorders|October 16, 2012
Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson diseaseM J Barrett, J Hagenah, V Dhawan, et al.Pageof 7