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22. A protein truncation test for Emery-Dreifuss muscular dystrophy (EMD): detection of N-terminal truncating mutations. de Koning Gans PA; Ginjaar I; Bakker E; Yates JR; den Dunnen JT Neuromuscul Disord; 1999 Jun; 9(4):247-50. PubMed ID: 10399752 [TBL] [Abstract][Full Text] [Related]
23. Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion. Fujimoto S; Ishikawa T; Saito M; Wada Y; Wada I; Arahata K; Nonaka I Neuropediatrics; 1999 Jun; 30(3):161-3. PubMed ID: 10480214 [TBL] [Abstract][Full Text] [Related]
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28. Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expression. Taylor J; Sewry CA; Dubowitz V; Muntoni F Neurology; 1998 Oct; 51(4):1116-20. PubMed ID: 9781539 [TBL] [Abstract][Full Text] [Related]
29. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Bione S; Maestrini E; Rivella S; Mancini M; Regis S; Romeo G; Toniolo D Nat Genet; 1994 Dec; 8(4):323-7. PubMed ID: 7894480 [TBL] [Abstract][Full Text] [Related]
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