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...

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Detalles Bibliográficos
Autores principales: Miere, Cristian, Hewitson, Heema, Wood, Victoria, Kadeva, Neli, Cornwell, Glenda, Codognotto, Stefano, Stephenson, Emma, Ilic, Dusko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Lab resource: Stem cell line
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

Internet

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

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