Elizabeth M Fisher

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.

Patrick Santens, Karin Peeters, Rik Vandenberghe, 2008, Human molecular genetics.

Graphical modelling of molecular networks underlying sporadic inclusion body myositis.

Thomas Thorne, Michael P H Stumpf, Michael G Hanna, 2013, Molecular bioSystems.