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Novel mutations in the emerin gene in Israeli families Communicated by Mark H. Paalman Online Citation: Human Mutation, Mutation in Brief #422 (2001) Online http://journals.wiley.com/1059-7794/pdf/mutation/422.pdf

2001; Wiley; Volume: 17; Issue: 6 Linguagem: Inglês

10.1002/humu.1139.abs

1098-1004

Yoram Nevo, Sarit Ahituv, Yuval Yaron, Merav Kedmi, Ruth Shomrat, Cyril Legum, Avi Orr‐Urtreger,

RNA modifications and cancer

Emery-Dreifuss Muscular Dystrophy (EMD or EDMD) is a rare X-linked recessive disorder, characterized by progressive muscle wasting and weakness, contractures, and cardiomyopathy, manifesting as heart block. Mutation analysis at the EMD gene locus was performed in 4 unrelated Israeli families with X-linked EMD and in one sporadic case. In the 4 families 4 different mutations were found, 3 of which were novel. These included two frame shift mutations in exon 2 (333delT and 412insA) and one base pair substitution at the consensus +1 donor splice in intron 5 (1429G→A). The fourth mutation in exon 6 (1675-1678delTCCG) has been previously described. No mutations were identified in the one sporadic case. Two of the three novel mutations were found in exon 2. A summary of the previously published mutations described in the EMD Mutation Database (http://www.path.cam.ac.uk/emd/) as well as the mutations described in our study suggest that the distribution of mutations in EMD gene is not entirely random and that exon 2 is prone to mutations. Hum Mutat 17:522, 2001. © 2001 Wiley-Liss, Inc.