Associated Papers
The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement Disorder.
Benger M et al.
Frontiers in Neurology, 2019
Molecular characterization of PRKN structural variations identified through whole-genome sequencing.
Bravo P et al.
Molecular Genetics & Genomic Medicine, 2018
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