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Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy

✍ Scribed by Patrizia Sabatelli; Giovanna Lattanzi; Andrea Ognibene; Marta Columbaro; Cristina Capanni; Luciano Merlini; Nadir M. Maraldi; Stefano Squarzoni


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
182 KB
Volume
24
Category
Article
ISSN
0148-639X

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## Communicated by Jiirgen Horst Mutations in the emerin gene, also referred to as the STA-or EMD-gene, have been found to be the cause of X-linked Emery-Dreifuss muscular dystrophy (EMD). For the present study an optimized set of primers was designed to amplify and sequence each of the six emerin