Back to search

Article

Allelic Diversity, de novo CAG Expansions, and Intergenerational Instability at the HTT Locus in a clinical sample of Huntington’s Disease from India

2025-03-04

Abstract excerpt

<h4>BACKGROUND</h4> Huntington’s disease (HD) is an inherited, neurodegenerative disorder, caused by the expansion of an unstable CAG repeat sequence in the HTT gene. The prevalence of HD, allelic diversity, rate of novel expansions, and the clinical correlates, vary across populations. <h4>OBJECTIVE</h4> We aimed to analyze the diversity of alleles, and their clinical correlates; and describe the mode of inherita...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
041b09e9-2287-5c09-870e-112a78d411a5
DOI
10.1101/2025.03.03.21260193
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Allelic Diversity, de novo CAG Expansions, and Intergenerational Instability at the HTT Locus in a clinical sample of Huntington’s Disease from IndiaDOI 10.1101/2025.03.03.21260193
Select a neighboring publication to make it the new centre.