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 - Université de Rennes Access content directly
Journal Articles Neuromuscular Disorders Year : 2016

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

L. Davignon
  • Function : Author
C. Chauveau
  • Function : Author
C. Julien
  • Function : Author
C. Dill
  • Function : Author
L. Duband-Goulet
  • Function : Author
E. Cabet
  • Function : Author
B. Buendia
  • Function : Author
A. Lilienbaum
M. Minot
  • Function : Author
A. Guichet
  • Function : Author
V. Allamand
N. Vadrot
  • Function : Author
L. Lazaro
  • Function : Author
J. Leroy
  • Function : Author
O. Dubourg
  • Function : Author
A. Ferreiro
  • Function : Author

Abstract

no abstract

Domains

Genetics
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Dates and versions

hal-01415936 , version 1 (13-12-2016)

Identifiers

Cite

L. Davignon, C. Chauveau, C. Julien, C. Dill, L. Duband-Goulet, et al.. 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. Neuromuscular Disorders, 2016, 26 (suppl 2), pp.S118--S119. ⟨10.1016/j.nmd.2016.06.121⟩. ⟨hal-01415936⟩
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