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                                       Details for article 3 of 18 found articles
 
 
  Cap disease caused by heterozygous deletion of the β-tropomyosin gene TPM2
 
 
Title: Cap disease caused by heterozygous deletion of the β-tropomyosin gene TPM2
Author: Lehtokari, Vilma-Lotta
Ceuterick-de Groote, Chantal
de Jonghe, Peter
Marttila, Minttu
Laing, Nigel G.
Pelin, Katarina
Wallgren-Pettersson, Carina
Appeared in: Neuromuscular disorders
Paging: Volume 17 (2007) nr. 6 pages 10 p.
Year: 2007
Contents:
Publisher: Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 3 of 18 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands