Author

Goncagül Mert

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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