Gene: CABP4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57010
Gene Symbol: CABP4
CABP4 		0.010 GeneticVariation disease BEFREE A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype. 20157620 2010