GeneticsOrphanet Journal of Rare DiseasesPeer-reviewed
Transcriptome analysis of atad3-null zebrafish embryos elucidates possible disease mechanisms
Shlomit Ezer, Nathan Ronin, Shira Yanovsky‐Dagan…·Tamar Harel
This study uses zebrafish atad3 knockout models to identify mitochondrial dysfunction as a key mechanism in ATAD3A-related human diseases.
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