Malformations of cortical developmentGene: PEX10
personal communication with Clinical Genetics team in North Thames GMC noting the association between Zellweger syndrome and cortical malformations inc band heterotopia
Created: 23 Apr 2018, 11:42 a.m.
Phenotypes for PEX10 were set to Disorders of peroxisome biogenesis; Peroxisome biogenesis disorder 6A (Zellweger), 614870; Peroxisome biogenesis disorder 6B, 614871
PEX10 was added to Malformations of cortical development panel. Sources: Expert Review Green,Literature
PEX10 was created by Louise Daugherty