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Neurogenetics|November 15, 2005
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patientSimona Lucioli, Klaus Hoffmeier, Rosalba Carrozzo, et al.Neurogenetics|March 25, 2000
Angelman syndrome: how many genes to remain silent?C Rougeulle, M LalandeNeurogenetics|March 25, 2000
The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophreniaO Wittekindt, A Jauch, E Burgert, et al.Neurogenetics|March 25, 2000
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory diseaseA Migheli, T Mongini, C Doriguzzi, et al.Neurogenetics|March 25, 2000
Characterization of the rat spinocerebellar ataxia type 3 geneI Schmitt, T Brattig, M Gossen, et al.Neurogenetics|March 25, 2000
A missense mutation in the SOD1 gene in patients with amyotrophic lateral sclerosis from the Kii Peninsula and its vicinity, JapanK Kikugawa, R Nakano, T Inuzuka, et al.Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.Neurogenetics|March 25, 2000
The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD Collaborative GroupM C Speer, G Worley, J F Mackey, et al.Neurogenetics|March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10qM C Speer, M A Pericak-Vance, J M Stajich, et al.Pageof 96