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Showing articles 0 to 6 of 6 Filter Applied: gene (Click to remove) Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene NEJM 342:1560-1567, Lucking,C.B.,et al, 2000 Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease) NEJM 329:241-245, Tsujino,S.,et al, 1993 Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene NEJM 329:96-101, Roa,B.B.,et al, 1993 Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993 Molecular Genetics of Duchenne and Becker Muscular Dystrophy J Pediatr 117:1-15, Darras,B.T., 1990 Showing articles 0 to 6 of 6