The spinocerebellar ataxias (SCAs) are clinically and genetically a heterogeneous group of neurodegenerative disorders. To date, eight different loci causing SCA have been identified: SCA1, SCA2, Machado-Joseph disease (MJD)/SCA3, SCA4, SCA5, SCA6, SCA7, and dentatorubropallidoluysian atrophy (DRPLA
β¦ LIBER β¦
Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India
β Scribed by Priyadarshi Basu; Biswanath Chattopadhyay; Prasanta K. Gangopadhaya; Subhas C. Mukherjee; Krishna K. Sinha; Shyamal K. Das; Susanta Roychoudhury; Partha P. Majumder; Nitai P. Bhattacharyya
- Publisher
- Springer
- Year
- 2000
- Tongue
- English
- Weight
- 65 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0340-6717
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