Associated Papers
From variant interpretation to structural discovery: A new Zinc-binding domain in PARS2.
Hoebeke C et al.
Mitochondrion, 2026
Intracranial calcifications simulating Aicardi-Goutières syndrome in PARS2-related mitochondrial disease.
Gerard A et al.
American Journal of Medical Genetics. Part A, 2024
Routine Diagnostics Confirm Novel Neurodevelopmental Disorders.
Jauss RT et al.
Genes, 2022
36553572 (PubMed )
Supplement: genes-13-02305-s001.zip › genes-2014296-supplementary.xlsx › Supplementary_Table_1
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