@article{davignon:hal-01415936,
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. and Chauveau, C. and Julien, C. and Dill, C. and Duband-Goulet, L. and Cabet, E. and Buendia, B. and Lilienbaum, A. and Rendu, J. and Minot, M. and Guichet, A. and Allamand, V. and Vadrot, N. and Faure, J. and Odent, S. and Lazaro, L. and Leroy, J. and Marcorelles, P. and Dubourg, O. and Ferreiro, A.},
URL = {https://univ-rennes.hal.science/hal-01415936},
JOURNAL = {Neuromuscular Disorders},
PUBLISHER = {Elsevier},
VOLUME = {26},
NUMBER = {suppl 2},
PAGES = {S118--S119},
YEAR = {2016},
MONTH = Oct, DOI = {10.1016/j.nmd.2016.06.121},
HAL_ID = {hal-01415936},
HAL_VERSION = {v1},
}