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5. A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies. Meola G; Sansone V; Radice S; Skradski S; Ptacek L Neuromuscul Disord; 1996 May; 6(3):143-50. PubMed ID: 8784800 [TBL] [Abstract][Full Text] [Related]
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12. The myotonic dystrophies. Thornton C Semin Neurol; 1999; 19(1):25-33. PubMed ID: 10711986 [TBL] [Abstract][Full Text] [Related]
13. Proximal myotonic myopathy: clinical, neuropathologic, and molecular genetic features. Eisenschenk S; Triggs WJ; Pearl GS; Rojiani AM Ann Clin Lab Sci; 2001 Apr; 31(2):140-6. PubMed ID: 11337902 [TBL] [Abstract][Full Text] [Related]
14. The expanding clinical and genetic spectrum of the myotonic dystrophies. Ricker K Acta Neurol Belg; 2000 Sep; 100(3):151-5. PubMed ID: 11098287 [TBL] [Abstract][Full Text] [Related]