9 results on '"Tang, Beisha"'
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2. Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia
3. Spinocerebellar ataxia type 6 in Mainland China: Molecular and clinical features in four families
4. A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family
5. The rs3756063 polymorphism is associated with SNCA methylation in the Chinese Han population
6. Association between polymorphism of COMT gene (Val158Met) with Alzheimer's disease: An updated analysis
7. SCA38 is rare in mainland China
8. Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population
9. C9orf72 hexanucleotide repeat expansion analysis in Chinese spastic paraplegia patients
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