Involvement of Mitochondrial Dysfunction in FOXG1 Syndrome

Autor: Victoria A. Bjerregaard, Amanda M. Levy, Mille S. Batz, Ravina Salehi, Mathis Hildonen, Trine B. Hammer, Rikke S. Møller, Claus Desler, Zeynep Tümer

Publikováno v: Bjerregaard, V A, Levy, A M, Batz, M S, Salehi, R, Hildonen, M, Hammer, T B, Møller, R S, Desler, C & Tümer, Z 2023, ' Involvement of Mitochondrial Dysfunction in FOXG1 Syndrome ', Genes, vol. 14, no. 2, 246 . https://doi.org/10.3390/genes14020246

FOXG1 (Forkhead box g1) syndrome is a neurodevelopmental disorder caused by a defective transcription factor, FOXG1, important for normal brain development and function. As FOXG1 syndrome and mitochondrial disorders have shared symptoms and FOXG1 reg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b99f66bc44aa98bba09bd40209560972
https://doi.org/10.3390/genes14020246