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Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients
BACKGROUND: Huntington disease (HD) is caused by an expanded CAG repeat in the HD gene. Although the length of the CAG repeat strongly correlates with the age-at-onset (AAO), AAO in HD individuals may differ dramatically in spite of similar expanded CAG repeat lengths. Additional genetic or environm...
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| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3433364/ https://ncbi.nlm.nih.gov/pubmed/22720673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-13-48 |
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