ITFE-CKKER: NEW THERAPEUTIC APPROACH TO THE MUSCULAR DYSTROPHY OF BECKER (DMB) (Q2041423)
Jump to navigation
Jump to search
Project Q2041423 in Italy
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | ITFE-CKKER: NEW THERAPEUTIC APPROACH TO THE MUSCULAR DYSTROPHY OF BECKER (DMB) |
Project Q2041423 in Italy |
Statements
1,618,074.93 Euro
0 references
3,236,149.85 Euro
0 references
50.0 percent
0 references
29 September 2016
0 references
1 November 2019
0 references
ITALFARMACO S.P.A.
0 references
FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO
0 references
OPIS S.R.L.
0 references
45°33'21.82"N, 9°12'50.44"E
0 references
LA DISTROFIA MUSCOLARE DI BECKER (DMB) UNA PATOLOGIA NEUROMUSCOLARE APPARTENENTE AL GRUPPO DELLE DISTROFINOPATIE, DI CUI LA DISTROFIA MUSCOLARE DI DUCHENNE (DMD) RAPPRESENTA LA FORMA PI GRAVE. LE DISTROFINOPATIE SONO CAUSATE DA MUTAZIONI A CARICO DEL GENE DELLA DISTROFINA, UNA PROTEINA FONDAMENTALE PER LA STABILIZZAZIONE DEL CITOSCHELETRO NELLE FIBRE MUSCOLARI SCHELETRICHE E CARDIACHE. LA DMB UNA MALATTIA RARA, DIAGNOSTICATA TRA I 10 E 30 ANNI DI ET, CHE COLPISCE I MASCHI, CON INCIDENZA D (Italian)
0 references
THE MUSCULAR DYSTROPHY OF THE BECKER (DMB) MUSCULAR DYSTROPHY BELONGING TO THE DISTROFINOPATIE GROUP, OF WHICH DUCHENNE MUSCULAR DYSTROPHY (DMD) IS IN THE FORM OF A SERIOUS IP. DISTROFINOPATIE IS CAUSED BY DISTRACTED MUTATIONS OF THE DYSTROPHIN GENE, A KEY PROTEIN FOR THE STABILISATION OF MUSCULO-SKELETAL FIBRES INTO SKELETAL FIBRES. DMB IS A RARE DISEASE, DIAGNOSED IN 10 TO 30 YEARS OF ET, WHICH AFFECTS MALES, WITH INCIDENCE D (English)
0 references
Identifiers
E76D17000080009
0 references