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12. 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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17. [A case of myotonic dystrophy showing proximal dominant muscle involvement but not myotonia]. Mihori A; Miyauchi H; Kaneda K; Nakayama M; Ono S; Shimizu N Rinsho Shinkeigaku; 1999 Apr; 39(4):461-4. PubMed ID: 10391974 [TBL] [Abstract][Full Text] [Related]
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20. Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMM. Sun C; Henriksen OA; Tranebjaerg L Clin Genet; 1999 Dec; 56(6):457-61. PubMed ID: 10665666 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]