Molecular typing of PrPres in human sporadic CJD brain tissue.
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A. Hill | G. Klug | V. Lewis | S. Collins
[1] R. Will,et al. A new prionopathy , 2008, Annals of neurology.
[2] T. Montine,et al. A novel human disease with abnormal prion protein sensitive to protease , 2008, Annals of neurology.
[3] C. Masters,et al. Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles , 2005, Neurology.
[4] H. Budka,et al. Molecular classification of sporadic Creutzfeldt-Jakob disease. , 2003, Brain : a journal of neurology.
[5] J. Kaldor,et al. Creutzfeldt–Jakob disease in Australia 1970–1999 , 2002, Neurology.
[6] P Brown,et al. Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects , 1999, Annals of neurology.