Muriel Perron
0000-0002-1558-8236
CNRS
3 papers found
Refreshing results…
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa
Glycogen Synthase Kinase 3 Regulates the Genesis of Displaced Retinal Ganglion Cells3
Yap haploinsufficiency leads to Müller cell dysfunction and late-onset cone dystrophy
Missing publications? Search for publications with a matching author name.