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Generation of KCL027 research grade human embryonic stem cell line carrying a mutation in the HTT gene
The KCL027 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the HTT gene encoding huntingtin (43 trinucleotide repeats; 21 for the normal allele). The ICM was isolated using laser microsurgery and plate...
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| 出版年: | Stem Cell Res |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Elsevier
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4823767/ https://ncbi.nlm.nih.gov/pubmed/27345982 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.scr.2016.01.008 |
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