CATALOGO DEI PRODOTTI DELLA RICERCA

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.

Brockington M.;Blake D. J.;PRANDINI, PAOLA;Brown S. C.;Torelli S.;Benson M. A.;Ponting C. P.;Estournet B.;Romero N. B.;Mercuri E.;Voit T.;Sewry C. A.;Guicheney P.;Muntoni F.

2001-01-01