Counting CAG repeats in the Huntington’s disease gene by restriction endonuclease EcoP15I cleavage
Huntington’s disease (HD) is a progressive neurodegenerative disorder with autosomal-dominant inheritance. The disease is caused by a CAG trinucleotide repeat expansion located in the first exon of the HD gene. The CAG repeat is highly polymorphic and varies from 6 to 37 repeats on chromosomes of un...
Uloženo v:
| Vydáno v: | Nucleic Acids Res |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2002
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC134256/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12177311/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/gnf082 |
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