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

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Bibliographic Details
Title: Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry.
Authors: Brimble, Elise1 (AUTHOR) elli.brimble@invitae.com, Reyes, Kathryn G.2 (AUTHOR), Kuhathaas, Kopika3 (AUTHOR), Devinsky, Orrin4 (AUTHOR), Ruzhnikov, Maura R. Z.5 (AUTHOR), Ortiz-Gonzalez, Xilma R.6 (AUTHOR), Scheffer, Ingrid7 (AUTHOR), Bahi-Buisson, Nadia8 (AUTHOR), Olson, Heather9 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 6/12/2023, Vol. 18 Issue 1, p1-10. 10p.
Database: Academic Search Ultimate
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Description
ISSN:17501172
DOI:10.1186/s13023-023-02745-y