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Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry

Document Type

Article

Author

Brimble, E.; Reyes, K.G.; Kuhathaas, K.; Devinsky, O.; Ruzhnikov, M.R.Z.; Ortiz-Gonzalez, X.R.; Scheffer, I.; Bahi-Buisson, N.; Olson, H.

Source

In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, December 2023, 18(1))

Subject

Language

English

ISSN

17501172

Online Access

EBSCOHost PDF Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Open Access (BioMed Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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