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authFullName_s : L. Lazaro

Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathy.

H. Rosas-Vargas , N. Bahi-Buisson , C. Philippe , J. Nectoux , B. Girard et al.
Journal of Medical Genetics, 2008, 45 (3), pp.172-8. ⟨10.1136/jmg.2007.053504⟩
Journal articles istex hal-00277624v1

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

L. Davignon , C. Chauveau , C. Julien , C. Dill , L. Duband-Goulet et al.
Neuromuscular Disorders, 2016, 26 (suppl 2), pp.S118--S119. ⟨10.1016/j.nmd.2016.06.121⟩
Journal articles hal-01415936v1