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optic atrophy
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UCHL1
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease
Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice
The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease
Alpha-synuclein has an altered conformation and shows a tight intermolecular interaction with ubiquitin in Lewy bodies
Isolation of PGP 9.5, a new human neurone-specific protein detected by high-resolution two-dimensional electrophoresis
OPA1
Extramitochondrial OPA1 and adrenocortical function
The effect of OPA1 on mitochondrial Ca���������� signaling
Mitochondrial dynamics and disease, OPA1
OPA3
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene
TMEM126A
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