4 results on '"Shan Jingli"'
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2. Oculopharyngeal Muscular Dystrophy: Phenotypic and Genotypic Studies in a Chinese Population
3. Novel Mitochondrial C15620A Variant may Modulate the Phenotype of Mitochondrial G11778A Mutation in a Chinese Family with Leigh Syndrome
4. Novel PANK2 gene mutations in two Chinese siblings with atypical pantothenate kinase-associated neurodegeneration
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