FERRERO, MARTA
FERRERO, MARTA
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Loss-of-function variants in CAPRIN1 in patients affected by autism spectrum disorder, language delay and intellectual disability with variable expressivity and incomplete penetrance
2020-01-01 Pavinato, L; Howe, JL; Carli, D; Agolini, E; Coviello, DA; Van de Laar, IMBH; Au, PYB; Di Gregorio, E; Giorgio, E; Pozzi, E; Ferrero, M; Cardaropoli, S; Delle Vedove, A; Salpietro, V; Zara, F; Novelli, A; Wirth, B; Ferrero, GB; Scherer, SW; Brusco, A
Unraveling molecular pathogenesis of SCA38, a novel autosomal dominant ataxia with a possible treatment
2015-01-01 Eleonora Di Gregorio; Marta Ferrero; Neftj Ragusa; Federica Gottardi; Paolo Costa; Adele Zoppo; Eriola Hoxha; Filippo Tempia; Loredana Boccone; Nico Mitro; Donatella Caruso; Alfredo Brusco; Barbara Borroni
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Loss-of-function variants in CAPRIN1 in patients affected by autism spectrum disorder, language delay and intellectual disability with variable expressivity and incomplete penetrance | 2020 | Pavinato, L; Howe, JL; Carli, D; Agolini, E; Coviello, DA; Van de Laar, IMBH; Au, PYB; Di Gregorio, E; Giorgio, E; Pozzi, E; Ferrero, M; Cardaropoli, S; Delle Vedove, A; Salpietro, V; Zara, F; Novelli, A; Wirth, B; Ferrero, GB; Scherer, SW; Brusco, A | |
| Unraveling molecular pathogenesis of SCA38, a novel autosomal dominant ataxia with a possible treatment | 2015 | Eleonora Di Gregorio; Marta Ferrero; Neftj Ragusa; Federica Gottardi; Paolo Costa; Adele Zoppo; Eriola Hoxha; Filippo Tempia; Loredana Boccone; Nico Mitro; Donatella Caruso; Alfredo Brusco; Barbara Borroni |