Distrofia muscolare: in copertina su ‘Human Mutation’ uno studio Cnr
(Availalble only in Italian) La rivista ‘Human Mutation’ ha dedicato la copertina di febbraio 2018 (volume 39, issue 2, pag. 266–280) all’articolo ‘A dystroglycan mutation (p.Cys667Phe) associated to muscle-eye-brain disease with multicystic leucodystrophy results...