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Analysis of the (CAG)n repeat causing Huntington's disease in a Mexican population

✍ Scribed by Ma Elisa Alonso; Petra Yescas; Bulmaro Cisneros; Claudia Martínez; Guadalupe Silva; Adriana Ochoa; Cecilia Montañez

Book ID
110887612
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
454 KB
Volume
51
Category
Article
ISSN
0009-9163

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## Communicated by Christine Van Broeckhoven Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized clinically by progressive motor impairment, cognitive decline, and emotional deterioration. The disease is caused by the abnormal expansion of a CAG trinucleotide