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Sequence-Level Analysis of the Major European Huntington Disease Haplotype
Huntington disease (HD) reflects the dominant consequences of a CAG-repeat expansion in HTT. Analysis of common SNP-based haplotypes has revealed that most European HD subjects have distinguishable HTT haplotypes on their normal and disease chromosomes and that ∼50% of the latter share the same majo...
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| Foilsithe in: | Am J Hum Genet |
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| Main Authors: | , , , , , , , , , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Elsevier
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4564985/ https://ncbi.nlm.nih.gov/pubmed/26320893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2015.07.017 |
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