Gene: SFXN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 94081
Gene Symbol: SFXN1
SFXN1 		0.010 GeneticVariation disease BEFREE Among them, HSP with thin corpus callosum and intellectual disability is a frequent subtype, often inherited as a recessive trait (ARHSP-TCC). 24337409 2014