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27. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. Pegoraro E; Mancias P; Swerdlow SH; Raikow RB; Garcia C; Marks H; Crawford T; Carver V; Di Cianno B; Hoffman EP Ann Neurol; 1996 Nov; 40(5):782-91. PubMed ID: 8957020 [TBL] [Abstract][Full Text] [Related]
28. Quadriceps myopathy: forme fruste of Becker muscular dystrophy. Sunohara N; Arahata K; Hoffman EP; Yamada H; Nishimiya J; Arikawa E; Kaido M; Nonaka I; Sugita H Ann Neurol; 1990 Nov; 28(5):634-9. PubMed ID: 2260849 [TBL] [Abstract][Full Text] [Related]
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31. An autosomal dominant type of congenital muscular dystrophy. Leyten QH; Gabreëls FJ; Joosten EM; Renier WO; Ter Laak HJ; Ter Haar BG; Stadhouders AM Brain Dev; 1986; 8(5):533-7. PubMed ID: 3799922 [TBL] [Abstract][Full Text] [Related]
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