Sfoglia per Rivista
Functional characterization of ryanodine receptor (RYR1) sequence variants using a metabolic assay in immortalized B-lymphocytes
2009-01-01 Zullo, A; Klingler, W; De Sarno, C; Ferrara, M; Fortunato, G; Perrotta, G; Gravino, E; Di Noto, R; Lehmann-Horn, F; Melzer, W; Salvatore, F; Carsana, A
Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: First evidence for an altered channel regulation by syntaxin-1A
2014-01-01 Soldovieri, Maria Virginia; Boutry-Kryza, Nadia; Milh, Mathieu; Doummar, Diane; Heron, Benedicte; Bourel, Emilie; Ambrosino, Paolo; Miceli, Francesco; De Maria, Michela; Dorison, Nathalie; Auvin, Stephane; Echenne, Bernard; Oertel, Julie; Riquet, Audrey; Lambert, Laetitia; Gerard, Marion; Roubergue, Anne; Calender, Alain; Mignot, Cyril; Taglialatela, Maurizio; Lesca, Gaetan
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Functional characterization of ryanodine receptor (RYR1) sequence variants using a metabolic assay in immortalized B-lymphocytes | 1-gen-2009 | Zullo, A; Klingler, W; De Sarno, C; Ferrara, M; Fortunato, G; Perrotta, G; Gravino, E; Di Noto, R; Lehmann-Horn, F; Melzer, W; Salvatore, F; Carsana, A | |
Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: First evidence for an altered channel regulation by syntaxin-1A | 1-gen-2014 | Soldovieri, Maria Virginia; Boutry-Kryza, Nadia; Milh, Mathieu; Doummar, Diane; Heron, Benedicte; Bourel, Emilie; Ambrosino, Paolo; Miceli, Francesco; De Maria, Michela; Dorison, Nathalie; Auvin, Stephane; Echenne, Bernard; Oertel, Julie; Riquet, Audrey; Lambert, Laetitia; Gerard, Marion; Roubergue, Anne; Calender, Alain; Mignot, Cyril; Taglialatela, Maurizio; Lesca, Gaetan |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile