Congenital muscular dystrophies (CMD) with reduced glycosylation of alpha-dystroglycan (alpha-DG) are a heterogeneous group of conditions associated with mutations in six genes encoding proven or putative glycosyltransferases.
Mercuri, E. M., Messina, S., Bruno, C., Mora, M., Pegoraro, E., Comi, G., D'amico, A., Aiello, C., Biancheri, R., Berardinelli, A., Boffi, P., Cassandrini, D., Laverda, A., Moggio, M., Morandi, L., Moroni, I., Pane, M., Pezzani, R., Pichiecchio, A., Pini, A., Minetti, C., Mongini, T., Mottarelli, E., Ricci, E., Ruggieri, A., Saredi, S., Scuderi, C., Tessa, A., Toscano, A., Tortorella, G., Trevisan, C., Uggetti, C., Vasco, G., Santorelli, F., Bertini, E. S., Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study, <<NEUROLOGY>>, 2009; 72 (21): 1802-1809. [doi:10.1212/01.wnl.0000346518.68110.60] [http://hdl.handle.net/10807/30810]
Autori: | ||
Titolo: | Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study | |
Digital Object Identifier (DOI): | http://dx.doi.org/10.1212/01.wnl.0000346518.68110.60 | |
Data di pubblicazione: | 2009 | |
Abstract: | Congenital muscular dystrophies (CMD) with reduced glycosylation of alpha-dystroglycan (alpha-DG) are a heterogeneous group of conditions associated with mutations in six genes encoding proven or putative glycosyltransferases. | |
Lingua: | Inglese | |
Rivista: | ||
Citazione: | Mercuri, E. M., Messina, S., Bruno, C., Mora, M., Pegoraro, E., Comi, G., D'amico, A., Aiello, C., Biancheri, R., Berardinelli, A., Boffi, P., Cassandrini, D., Laverda, A., Moggio, M., Morandi, L., Moroni, I., Pane, M., Pezzani, R., Pichiecchio, A., Pini, A., Minetti, C., Mongini, T., Mottarelli, E., Ricci, E., Ruggieri, A., Saredi, S., Scuderi, C., Tessa, A., Toscano, A., Tortorella, G., Trevisan, C., Uggetti, C., Vasco, G., Santorelli, F., Bertini, E. S., Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study, <<NEUROLOGY>>, 2009; 72 (21): 1802-1809. [doi:10.1212/01.wnl.0000346518.68110.60] [http://hdl.handle.net/10807/30810] | |
Appare nelle tipologie: | Articolo in rivista, Nota a sentenza |