Author:
Magri Francesca,Govoni Alessandra,D’Angelo Maria Grazia,Del Bo Roberto,Ghezzi Serena,Sandra Gandossini,Turconi Anna Carla,Sciacco Monica,Ciscato Patrizia,Bordoni Andreina,Tedeschi Silvana,Fortunato Francesco,Lucchini Valeria,Bonato Sara,Lamperti Costanza,Coviello Domenico,Torrente Yvan,Corti Stefania,Moggio Maurizio,Bresolin Nereo,Comi Giacomo Pietro
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Reference44 articles.
1. Davies KE, Smith TJ, Bundey S, Read AP, Flint T, Bell M, Speer A (1988) Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome. J Med Genet 25:9–13
2. Comi GP, Prelle A, Bresolin N, Moggio M, Bardoni A, Gallanti A, Vita G, Toscano A, Ferrò MT, Bordoni A et al (1994) Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates. Brain 117:1–14
3. Beggs AH, Hoffman EP, Snyder JR, Arahata K, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel LM (1991) Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies. Am J Hum Genet 49:54–67
4. Béroud C, Tuffery-Giraud S, Matsuo M, Hamroun D, Humbertclaude V, Monnier N, Moizard MP, Voelckel MA, Calemard LM, Boisseau P, Blayau M, Philippe C, Cossée M, Pagès M, Rivier F, Danos O, Garcia L, Claustres M (2007) Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy. Hum Mutat 28:196–202
5. Emery AE (1994) Some unanswered questions in Duchenne muscular dystrophy. Neuromuscul Disord 4:301–303
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