Gene: AGRN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 375790
Gene Symbol: AGRN
AGRN 		0.500 GermlineCausalMutation disease ORPHANET LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin. 22205389 2012
Entrez Id: 375790
Gene Symbol: AGRN
AGRN 		0.500 GermlineCausalMutation disease ORPHANET Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. 19631309 2009
Entrez Id: 375790
Gene Symbol: AGRN
AGRN 		0.500 Biomarker disease CTD_human