ArticleHuman cell2024

Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9A.

Maryam Alowaysi et al.PubMed ↗Full text ↗Publisher ↗

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