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Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase
Age at onset of Huntington disease, an inherited neurodegenerative disorder, is influenced by the size of the disease-causing CAG trinucleotide repeat expansion in HTT and by genetic modifier loci on chromosomes 8 and 15. Stratifying by modifier genotype, we have examined putamen volume, total motor...
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| Published in: | Am J Hum Genet |
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| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Elsevier
2018
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6128248/ https://ncbi.nlm.nih.gov/pubmed/30122542 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2018.07.017 |
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