Expanding genotype-phenotype correlations in FOXG1 syndrome: results from a patient registry
Brimble, Elise, Reyes, Kathryn G, Kuhathaas, Kopika, Devinsky, Orrin, Ruzhnikov, Maura R Z, Ortiz-Gonzalez, Xilma R, Scheffer, Ingrid, Bahi-Buisson, Nadia, Olson, Heather
Published in Orphanet journal of rare diseases (12.06.2023)
Published in Orphanet journal of rare diseases (12.06.2023)
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