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                                       Details for article 15 of 19 found articles
 
 
  The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence
 
 
Title: The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence
Author: Lehtokari, Vilma-Lotta
Greenleaf, Rebecca S.
DeChene, Elizabeth T.
Kellinsalmi, Mutsumi
Pelin, Katarina
Laing, Nigel G.
Beggs, Alan H.
Wallgren-Pettersson, Carina
Appeared in: Neuromuscular disorders
Paging: Volume 19 (2009) nr. 3 pages 3 p.
Year: 2009
Contents:
Publisher: Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 15 of 19 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands