ERDA1, expanded repeat domain, CAG/CTG 1, 9030

N. diseases: 16; N. variants: 0
Disease: Parkinson Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 Biomarker disease BEFREE Our results demonstrate that unstable CAG/CTG expansions corresponding to uncloned or cloned sequences (ERDA1, CTG18.1) are not involved in the etiology of rare familial case of PD with genetic anticipation.Am.J. Med.Genet.(Neuropsychiatr.Genet.)88:738-741, 1999 10581499 1999