Publication | Closed Access
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease
72
Citations
16
References
1999
Year
Mendelian DisorderFamilial ParkinsonGenetic DisorderGeneticsInherited Metabolic DiseaseIle93met MutationPathologyDisease Gene IdentificationMedicineEuropean Cases
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