Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population
| Autor: | Goel, Divya, Suroliya, Varun, Shamim, Uzma, Mathur, Aradhna, Faruq, Mohammed * |
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| Zdroj: | In eNeurologicalSci December 2019 17 |
| Databáze: | ScienceDirect |
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