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10. History and current difficulties in classifying inherited myopathies and muscular dystrophies. Mathis S; Tazir M; Magy L; Duval F; Le Masson G; Duchesne M; Couratier P; Ghorab K; Solé G; Lacoste I; Goizet C; Vallat JM J Neurol Sci; 2018 Jan; 384():50-54. PubMed ID: 29249377 [TBL] [Abstract][Full Text] [Related]
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13. [Polymorphism of exon 4 in the CANP-3 gene in patients with primary myopathies]. Lipatova NA; Krakhmaleva IN; Shishkin SS; Shakhovskaia NI; Podnikova NI; Lunga IN; Tarksh MA; Gerasimova NL Genetika; 1999 Dec; 35(12):1713-7. PubMed ID: 10687099 [TBL] [Abstract][Full Text] [Related]
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16. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567 [TBL] [Abstract][Full Text] [Related]
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