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Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy

✍ Scribed by Maria Hoeltzenbein; Thomas Karow; Joern A Zeller; Rolf Warzok; Karin Wulff; Marlies Zschiesche; Falko H Herrmann; Wolfgang Große-Heitmeyer; Manfred S Wehnert


Book ID
117671010
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
155 KB
Volume
9
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