Gene: C19orf12 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83636
Gene Symbol: C19orf12
C19orf12 		0.010 GeneticVariation phenotype BEFREE Patients from 13 different families having progressive motor symptoms with irritative pyramidal signs and brain iron accumulation were screened for C19orf12 gene variants. 31804703 2019