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Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred.
Published in:
2011
By:
- Pietroboni AM;
- Fumagalli GG;
- Ghezzi L;
- Fenoglio C;
- Cortini F;
- Serpente M;
- Cantoni C;
- Rotondo E;
- Corti P;
- Carecchio M;
- Bassi M;
- Bresolin N;
- Galbiati D;
- Galimberti D;
- Scarpini E
Publication type:
Journal Article
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
Published in:
2011
By:
- Villa C;
- Ghezzi L;
- Pietroboni AM;
- Fenoglio C;
- Cortini F;
- Serpente M;
- Cantoni C;
- Ridolfi E;
- Marcone A;
- Benussi L;
- Ghidoni R;
- Jacini F;
- Arighi A;
- Fumagalli GG;
- Mandelli A;
- Binetti G;
- Cappa S;
- Bresolin N;
- Scarpini E;
- Galimberti D
Publication type:
journal article