Disease: Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842984
Disease: Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k 		0.200 Biomarker disease MGD Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy. 25860513 2015