Human iPSC lines from a Christianson syndrome patient with NHE6 W523X mutation, a biologically-related control, and CRISPR/Cas9 gene-corrected isogenic controls

Loss-of-function mutations in Na+/H + exchanger 6 (NHE6) (also termed SLC9A6) cause the X-linked neurogenetic disorder Christianson syndrome (CS). Using peripheral blood mononuclear cells, we developed induced pluripotent stem cell (iPSC) lines from a patient with the NHE6 nonsense mutation c.1569G...

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Detalles Bibliográficos
Autores principales: Ma, Li, Schmidt, Michael, Morrow, Eric M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375322/
https://www.ncbi.nlm.nih.gov/pubmed/34182254
http://dx.doi.org/10.1016/j.scr.2021.102435

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375322/
https://www.ncbi.nlm.nih.gov/pubmed/34182254
http://dx.doi.org/10.1016/j.scr.2021.102435

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