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Article

Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population.

The Indian journal of medical research - 1 Feb 2015

Faruq Mohammed, Srivastava Achal Kumar, Singh Suman, Gupta Rohit, Dada Tanuj, Garg Ajay, Behari Madhuri, Mukerji Mitali

Abstract excerpt

BACKGROUND & OBJECTIVES: Spinocerebellar ataxia 7 (SCA7) is a rare form of neurodegenerative disorder with the clinical manifestation of cerebellar ataxia and retinal degeneration. In this study we describe the clinico-genetic characteristics of nine SCA7 families of Indian origin and cross compare these with other available worldwide studies. METHODS: Thirty five individuals from nine SCA7 families were...

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Identifiers

PMID: 25900954
DOI: 10.4103/0971-5916.155556
PMCID: PMC4418155

Genes

ATXN7

Provenance

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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