Role of Dynamic and Mitochondrial Mutations in Neurodegenerative Diseases with Ataxia: Lower Repeats and LNAs at Multiple Loci as Alternative Pathogenesis

Author:

Gul Lone Waseem,Poornima Subhadra,Meena Angmuthu Kanikannan,Rao Kaipa Prabhakar,Hasan Qurratulain

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,General Medicine

Reference40 articles.

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2. Al-Ramahi I, Perez AM, Lim J et al (2007) dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1. PLoS Genet Am J Hum Genet 66(3):830–840

3. Bahl S, Virdi K, Mittal U et al (2005) Evidence of a common founder for SCA12 in the Indian population. Ann Hum Genet 69:528–534 (9419710273)

4. Baskaran S, Brahmachari V (2000) Chromosomal fragility and human genetic disorders. Indian J Clin Biochem 15(Suppl 1):145–157

5. Basu P, Chattopadhyay B, Gangopadhaya PK (2000) 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. Hum Genet 106(6):597–604

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