Publication | Closed Access
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia
37
Citations
38
References
2017
Year
Mendelian DisorderMitochondrial FunctionMitochondrial DysfunctionMedicineGeneticsGenetic DisorderMitochondrial MedicineMolecular GeneticsRecessive MutationCell BiologyExosc3 Associates
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