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Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS. [electronic resource] by
- Asante, Emmanuel A
- Grimshaw, Andrew
- Smidak, Michelle
- Jakubcova, Tatiana
- Tomlinson, Andrew
- Jeelani, Asif
- Hamdan, Shyma
- Powell, Caroline
- Joiner, Susan
- Linehan, Jacqueline M
- Brandner, Sebastian
- Wadsworth, Jonathan D F
- Collinge, John
Producer: 20160404
In:
PLoS pathogens vol. 11
Availability: No items available.
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Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation). [electronic resource] by
- Barbanti, P
- Fabbrini, G
- Salvatore, M
- Petraroli, R
- Cardone, F
- Maras, B
- Equestre, M
- Macchi, G
- Lenzi, G L
- Pocchiari, M
Producer: 19961122
In:
Neurology vol. 47
Availability: No items available.
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