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L. Davignon
L. Davignon
Paris Diderot University
Diabetes mellitus
Genetics
Biology
Cell biology
Transcription Coactivator
2
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1
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0
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CONGENITAL MYOPATHIES: GENERAL AND RYR1
2018
Neuromuscular Disorders
Isabelle Duband-Goulet
F. Catervi
Eva Cabet
L. Davignon
Casie A. Genetti
T. Gidaro
A. Koparir
S. Coppen
E. Pierce-Hoffman
Alan H. Beggs
L. Servais
Ana Ferreiro
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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
2016
Neuromuscular Disorders
L. Davignon
C. Chauveau
C. Julien
C. Dill
Isabelle Duband-Goulet
Eva Cabet
Brigitte Buendia
Alain Lilienbaum
John Rendu
M. Minot
Agnès Guichet
Valérie Allamand
Nathalie Vadrot
Julien Fauré
Sylvie Odent
L. Lazaro
J. Leroy
Pascale Marcorelles
O. Dubourg
Ana Ferreiro
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