A rapid and efficient method for the detection of point mutations of the human prion protein gene (PRNP) by direct sequencing
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference21 articles.
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2. Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan;Journal of Human Genetics;2009-05-15
3. Reference materials for the evaluation of pre-mortem variant Creutzfeldt?Jakob disease diagnostic assays;Vox Sanguinis;2007-03-02
4. Prion protein gene M129 allele is a risk factor for Alzheimer’s disease;Journal of Neural Transmission;2006-08-08
5. Cellular isoform of the prion protein PrPc in human intestinal cell lines: Genetic polymorphism at codon 129, mRNA quantification and protein detection in lipid rafts;Cell Biology International;2006-06
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