Gene: PDXP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57026
Gene Symbol: PDXP
PDXP 		0.010 GeneticVariation disease BEFREE These mutations cause a loss of PLP function leading to a histopathological and clinical phenotype common to both PMS and genetic CNS disorders, like hereditary spastic paraplegias. 29970109 2018