Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a PEX3 defect: Case report and literature review

Publication date: December 2020Source: Molecular Genetics and Metabolism Reports, Volume 25Author(s): Whiwon Lee, Gregory Costain, Susan Blaser, Susan Walker, Christian R. Marshall, Hernan Gonorazky, Michal Inbar-Feigenberg

Source: Molecular Genetics and Metabolism Reports - October 20, 2020 Category: Genetics & Stem Cells Source Type: research