Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's Disease. Fant A, Trova S, Monfrini E, Treves G, et al. Mov Disord 2025 Aug 30. doi: 10.1002/mds.70027.

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Fant A, Trova S, Monfrini E, Treves G, et al. Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's Disease. Mov Disord 2025 Aug 30. doi: 10.1002/mds.70027.
PMID: 40884420