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A mutation in the X-linked Emery–Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy

✍ Scribed by Stanislav Vohanka; Michal Vytopil; Josef Bednarik; Zdenek Lukas; Zdenek Kadanka; Jiri Schildberger; Roberta Ricotti; Silvia Bione; Daniela Toniolo


Book ID
117669382
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
299 KB
Volume
11
Category
Article
ISSN
0960-8966

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Six novel mutations in the emerin gene c
✍ Karin Wulff; Julia E. Parrish; Falko H. Herrmann; Manfred Wehnert 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 150 KB 👁 3 views

## 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