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Generation of KCL029 research grade human embryonic stem cell line carrying a mutation in WAS gene
The KCL029 human embryonic stem cell line was derived from an embryo donated for research that carried a c.814 T > C mutation in the WAS gene, which is linked to the Wiskott-Aldrich syndrome, a rare, inherited, X-linked, recessive disease characterized by immune dysregulation and microthrombocyto...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757721/ https://www.ncbi.nlm.nih.gov/pubmed/27345811 http://dx.doi.org/10.1016/j.scr.2015.12.040 |