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

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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Veröffentlicht in:Neuromuscular disorders : NMD 2016-10, Vol.26 (suppl 2), p.S118-S119
Hauptverfasser: 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, L, Leroy, J, Marcorelles, P, Dubourg, O, Ferreiro, A
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Genetics
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Neurology
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container_end_page S119
container_issue suppl 2
container_start_page S118
container_title Neuromuscular disorders : NMD
container_volume 26
creator 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, L
Leroy, J
Marcorelles, P
Dubourg, O
Ferreiro, A
description
doi_str_mv 10.1016/j.nmd.2016.06.121
format Article
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source ScienceDirect Journals (5 years ago - present)
subjects Genetics
Life Sciences
Neurology
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
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