A novel RRM2B mutation associated with mitochondrial DNA depletion syndrome.
Fumagalli M, Ronchi D, Bedeschi MF, Manini A, Cristofori G, Mosca F, Dilena R, Sciacco M, Zanotti S, Piga D, Ardissino G, Triulzi F, Corti S, Comi GP, Salviati L.
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Mol Genet Metab Rep. 2022 Jun 18;32:100887. doi: 10.1016/j.ymgmr.2022.100887. eCollection 2022 Sep.
Mol Genet Metab Rep. 2022.
PMID: 35756861
Free PMC article.