MRS2, magnesium transporter MRS2, 57380

N. diseases: 11; N. variants: 2
Disease: Deuteranomaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3887938
Disease: Deuteranomaly
Deuteranomaly 		0.010 Biomarker disease BEFREE Corticobasal degeneration can have a familial presentation; the role of MRS2 and ZHX2 gene products in CBD should be further investigated. 23867865 2013