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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 28, 2010
Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP geneA Alzualde, F Moreno, P Martínez-Lage, et al.
Neurology|May 11, 2005
A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron diseaseJ J Zarranz, I Ferrer, E Lezcano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2005
Phenotypic variability in familial prion diseases due to the D178N mutationJ J Zarranz, A Digon, B Atarés, et al.
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