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                                       Details for article 6 of 20 found articles
 
 
  A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
 
 
Title: A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
Author: Vorgerd, Matthias
van der Ven, Peter F.M.
Bruchertseifer, Vera
Löwe, Thomas
Kley, Rudolf A.
Schröder, Rolf
Lochmüller, Hanns
Himmel, Mirko
Koehler, Katrin
Fürst, Dieter O.
Huebner, Angela
Appeared in: The American journal of human genetics
Paging: Volume 77 (2005) nr. 2 pages 8 p.
Year: 2005
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 6 of 20 found articles
 
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