IFT52, intraflagellar transport 52, 51098

N. diseases: 67; N. variants: 2
Disease: Retinal Diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		0.010 GeneticVariation group BEFREE We herein aim to study the impact of IFT52 mutations in retinopathies. 30242358 2018