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Navegación por Autor Ravazzolo, Roberto
Mostrando resultados 1 a 2 de 2
Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
openAccess | | ene-2016 | ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism | Panza, Emanuele; Escamilla-Honrubia, Juan Manuel; Marco-Marín, Clara CSIC ORCID; Gougeard, Nadine CSIC ORCID; De Michele, Giuseppe; Brescia Morra, Vincenzo; Liguori, Rocco; Salviati, Leonardo; Donati, Maria Alice; Cusano, Roberto; Pippucci, Tommaso; Ravazzolo, Roberto; Nemeth, Andrea H; Smithson, Sarah; Davies, Sally; Hurst, Jane A; Bordo, Domenico; Rubio, Vicente CSIC ORCID ; Seri, Marco | artículo |
openAccess | | 2006 | Crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1) | Conti, Valerio; Aghaie, Asadollah; Cilli, Michele; Martín, Natalia; Caridi, Gianluca; Musante, Luca; Candiano, Giovanni; Castagna, Maura; Fairén, Alfonso CSIC; Ravazzolo, Roberto; Guenet, Jean-Louis; Puliti, Aldamaria | artículo |