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Article

Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India.

Neuroscience letters - 17 Jul 2003

Chattopadhyay Biswanath, Ghosh Subho, Gangopadhyay Prasanta K, Das Shaymal K, Roy T, Sinha Krishna K, Jha Dilip K, Mukherjee Subhash C, Chakraborty Ambar, Singhal Bhim S, Bhattacharya Anup K, Bhattacharyya Nitai P

Abstract excerpt

To identify the genetic modifier(s) that might alter the age at onset in Huntington's disease (HD) we have analyzed variations in GluR6 kainate receptor (GluR6), CA150 gene, Delta2642 and polymorphic CCG repeat variation in huntingtin (htt) gene in 77 HD patients and normal individuals. In addition, variation in the RAI1 gene was analyzed in 30 spinocerebellar ataxia (SCA2) patients and normal individuals to show...

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Identifiers

PMID: 12821179
DOI: 10.1016/s0304-3940(03)00436-1

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RAI1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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