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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

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https://hal-univ-rennes1.archives-ouvertes.fr/hal-01415936
Contributor : Laurent Jonchère <>
Submitted on : Tuesday, December 13, 2016 - 5:32:12 PM
Last modification on : Wednesday, August 19, 2020 - 11:17:21 AM

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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, Elsevier, 2016, 26 (suppl 2), pp.S118--S119. ⟨10.1016/j.nmd.2016.06.121⟩. ⟨hal-01415936⟩

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