Transcriptome analysis of atad3-null zebrafish embryos elucidates possible disease mechanisms
Shlomit Ezer, Nathan Ronin, Shira Yanovsky‐Dagan, Shahar Rotem‐Bamberger, Orli Halstuk, Yair Wexler, Zohar Ben-Moshe, Inbar Plaschkes, Hadar Benyamini, Ann Saada, Adi Inbal, Tamar Harel
This study uses zebrafish atad3 knockout models to identify mitochondrial dysfunction as a key mechanism in ATAD3A-related human diseases.
Orphanet Journal of Rare Diseases · Apr 15, 2025Peer-reviewedGenetics