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CCDC88C variants are associated with focal epilepsy and genotype–phenotype correlation

Document Type

Article

Author

Chen, Y.-J.; Jin, L.; Liu, X.-R.; Liao, W.-P.; Li, B.; Chen, Y.-J.; Wang, W.-J.; Zou, D.-F.; Luo, J.-X.; Jin, P.-Y.

Source

In: Clinical Genetics. (Clinical Genetics, April 2024, 105(4):397-405)

Subject

Language

English

ISSN

13990004
00099163

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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