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                                       Details for article 246 of 451 found articles
 
 
  Loss-of-function mutation of TRIP4 causes a novel form of congenital muscle disease and reveals the transcription coactivator ASC-1 as a new regulator of skeletal myogenesis
 
 
Title: Loss-of-function mutation of TRIP4 causes a novel form of congenital muscle disease and reveals the transcription coactivator ASC-1 as a new regulator of skeletal myogenesis
Author: Davignon, L.
Chauveau, C.
Julien, C.
Dill, C.
Duband-Goulet, I.
Cabet, E.
Buendia, B.
Lilienbaum, A.
Rendu, J.
Minot, M.
Guichet, A.
Allamand, V.
Vadrot, N.
Fauré, J.
Odent, S.
Lazaro, L.
Leroy, J.
Marcorelles, P.
Dubourg, O.
Ferreiro, A.
Appeared in: Neuromuscular disorders
Paging: Volume 26 (2016) nr. S2 pages 2 p.
Year: 2016
Contents:
Publisher: Published by Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 246 of 451 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands