Amina Belhadj

Whole exome sequencing of an Algerian Parkinson’s disease cohort: an exploratory study identifying rare variants in putative candidate genes

The genetic diversity of Parkinson’s disease in the Algerian population is investigated using whole exome sequencing and GLUD2 emerges as a particularly compelling candidate requiring functional validation for future investigations, highlighting the value of whole exome sequencing for the identification of rare variant...