Sep 2026
Clinical and genetic findings in Parkinson’s disease in a Turkish cohort: a retrospective exome sequencing study
The characterization of prominent VUS in OMIM-associated genes and a novel LRRK2 structural variant undetected by routine MLPA highlights the evolving complexity of PD genetics and the critical need for integrating comprehensive, read-depth-based CNV analysis into standard pipelines.
Sezin Canbek, M. F. Gulseven, Goncagül Mert et al.
· Neurogenetics · 0 citations