Briguet A

References (2)

Title : A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome - Abicht_2002_Brain_125_1005
Author(s) : Abicht A , Stucka R , Schmidt C , Briguet A , Hopfner S , Song IH , Pongratz D , Muller-Felber W , Ruegg MA , Lochmuller H
Ref : Brain , 125 :1005 , 2002
Abstract : Abicht_2002_Brain_125_1005
ESTHER : Abicht_2002_Brain_125_1005
PubMedSearch : Abicht_2002_Brain_125_1005
PubMedID: 11960891

Title : The Ets transcription factor GABP is required for postsynaptic differentiation in vivo - Briguet_2000_J.Neurosci_20_5989
Author(s) : Briguet A , Ruegg MA
Ref : Journal of Neuroscience , 20 :5989 , 2000
Abstract : Briguet_2000_J.Neurosci_20_5989
ESTHER : Briguet_2000_J.Neurosci_20_5989
PubMedSearch : Briguet_2000_J.Neurosci_20_5989
PubMedID: 10934247