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Genetic Counseling in Huntington's Disease: Potential New Challenges on Horizon?
Huntington's disease (HD) is a rare, hereditary, neurodegenerative and dominantly transmitted disorder affecting about 10 out of 100,000 people in Western Countries. The genetic cause is a CAG repeat expansion in the huntingtin gene (HTT), which is unstable and may further increase its length i...
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| 出版年: | Front Neurol |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6503085/ https://ncbi.nlm.nih.gov/pubmed/31114543 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.00453 |
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