Loss-of-function mutation of TRIP4 causes a novel form of...

Neuromuscular Disorders 2016 / 10 Vol. 26

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

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,
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Volume:
26
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2016.06.121
Date:
October, 2016
File:
PDF, 208 KB
english, 2016
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