MRS2, magnesium transporter MRS2, 57380

N. diseases: 11; N. variants: 2
Disease: Demyelinating Diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011303
Disease: Demyelinating Diseases
Demyelinating Diseases 		0.200 Biomarker group RGD A mutation in the gene encoding mitochondrial Mg²+ channel MRS2 results in demyelination in the rat. 21253565 2011