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
,
C. Chauveau
,
C. Julien
(1)
,
C. Dill
,
L. Duband-Goulet
,
E. Cabet
,
B. Buendia
,
A. Lilienbaum
,
J. Rendu
(2)
,
M. Minot
,
A. Guichet
,
V. Allamand
(3)
,
N. Vadrot
,
J. Faure
(2)
,
S. Odent
(4, 5)
,
L. Lazaro
,
J. Leroy
,
P. Marcorelles
(6)
,
O. Dubourg
,
A. Ferreiro
L. Davignon
- Function : Author
C. Chauveau
- Function : Author
C. Dill
- Function : Author
L. Duband-Goulet
- Function : Author
E. Cabet
- Function : Author
B. Buendia
- Function : Author
A. Lilienbaum
- Function : Author
- PersonId : 750102
- IdHAL : alain-lilienbaum
- ORCID : 0000-0002-6437-3186
M. Minot
- Function : Author
A. Guichet
- Function : Author
V. Allamand
- Function : Author
- PersonId : 1178516
- IdHAL : valerie-allamand
- ORCID : 0000-0001-8997-9742
N. Vadrot
- Function : Author
L. Lazaro
- Function : Author
J. Leroy
- Function : Author
O. Dubourg
- Function : Author
A. Ferreiro
- Function : Author
Abstract
no abstract