论文信息 - LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact - 字舞流文

LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact

K. Kandaswamy | P. Bauer | N. Ameziane | A. Rolfs | C. Beetz | M. Alfadhel | Z. Al-Hassnan | R. Boustany | Ruslan Al-Ali | A. Westenberger | O. Paknia | F. Al Mutairi | V. Skrahina | Nadia Alhashmi | M. Alsayed