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                                       Details for article 7 of 27 found articles
 
 
  De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy
 
 
Title: De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy
Author: Durling, H.J
Reilich, P
Müller-Höcker, J
Mendel, B
Pongratz, D
Wallgren-Pettersson, C
Gunning, P
Lochmüller, H
Laing, N.G
Appeared in: Neuromuscular disorders
Paging: Volume 12 (2002) nr. 10 pages 5 p.
Year: 2002
Contents:
Publisher: Elsevier Science B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 7 of 27 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands