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Huntington disease or HD is a progressive, fatal neurodegenerative disorder inherited in an autosomal dominant pattern.PathophysiologyIt is caused by expansion of the CAG trinucleotide repeat in the HTT gene on chromosome 4 (4p16.3), producing an abnormal huntingtin protein with an expanded polyglutamine tract. This misfolded protein disrupts cellular function, leading to neuronal death. Normal alleles have ≤26 repeats, 27–35 are intermediate (risk of expansion), 36–39 show reduced penetrance,...

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Related Experiment Video

Updated: Jun 19, 2026

Building Langmuir Probes and Emissive Probes for Plasma Potential Measurements in Low Pressure, Low Temperature Plasmas

Building Langmuir Probes and Emissive Probes for Plasma Potential Measurements in Low Pressure, Low Temperature Plasmas

Published on: May 25, 2021

In memoriam: Steven A. Huesing (1944-2009)

R Haux¹, N M Lorenzi, K C Lun

¹University of Braunschweig and Medical School, Hannover, Germany. Reinhold.Haux@plri.de, www.plri.de

Yearbook of Medical Informatics

|October 27, 2009

Summary

No abstract available in PubMed .

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