Publication | Closed Access
Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype
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Citations
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References
1995
Year
BiologyGenetic DisorderMedicineGeneticsOlivopontocerebellar AtrophyDegenerative DiseaseDisease Gene IdentificationUnique PhenotypeImmunocytochemical FeaturesNeuropathologyNeuromuscular PathologyNeurogenetics
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