Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Rebekah Lifer"'
Autor:
Kirsty R. Erickson, Rebekah Lifer, Jonathan K. Merritt, Zeljka Miletic Lanaghan, Mark D. Does, Karthik Ramadass, Bennett A. Landman, Laurie E. Cutting, Jeffrey L. Neul
FOXG1 Syndrome (FS) is a devastating neurodevelopmental disorder that is caused by a heterozygous loss-of-function (LOF) mutation of the FOXG1 gene, which encodes a transcriptional regulator important for telencephalic brain development. People with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d408a73ed2e9b4a4967836a5afe1030a
https://doi.org/10.1101/2022.03.29.486318
https://doi.org/10.1101/2022.03.29.486318
