Mutations of the prion protein (PrP) gene are present in patients with Gerstmann-Straussler-Scheinker syndrome (GSS), familial Creutzfeldt-Jakob disease (CJD), and fatal familial insomnia (FFI). We developed a denaturing gradient gel electrophoresis (DGGE) strategy that readily identifies point muta
β¦ LIBER β¦
Detection of p53 point mutations by double-gradient, denaturing gradient gel electrophoresis
β Scribed by Cecilia Gelfi; Sabina C. Righetti; Franco Zunino; Gabriella Della Torre; Marco A. Pierotti; Prof. Pier Giorgio Righetti
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 718 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0173-0835
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