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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

Document Type

Article

Author

Alowaysi, M.; Al-Shehri, M.; Badkok, A.; Attas, H.; Aboalola, D.; Baadhaim, M.; Alzahrani, H.; Daghestani, M.; Zakri, S.; Aouabdi, S.; Alsayegh, K.; Zia, A.; Tegner, J.; Al-Ghamdi, K.; Al-Ghamdi, A.

Source

In: Human Cell. (Human Cell, March 2024, 37(2):502-510)

Subject

Language

English

ISSN

17490774
09147470

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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