Generation of KCL025 research grade human embryonic stem cell line carrying a mutation in NF1 gene

The KCL025 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation in the NF1 gene encoding neurofibromin (c.3739–3742 ΔTTTG). Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and...

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Detalles Bibliográficos
Autores principales: 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/PMC4823762/
https://www.ncbi.nlm.nih.gov/pubmed/27345978
http://dx.doi.org/10.1016/j.scr.2016.01.009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823762/
https://www.ncbi.nlm.nih.gov/pubmed/27345978
http://dx.doi.org/10.1016/j.scr.2016.01.009

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