The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's diseaseChin-Song Lu, Vincenzo Bonifati, Erik Simons et al.|Parkinsonism & Related Disorders|2005Cited by 79
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrumYanick J. Crow, Axel Panzer, Roberta Battini et al.|American Journal of Medical Genetics Part A|2020Cited by 29
A Novel Homozygous <scp><i>VPS11</i></scp> Variant May Cause Generalized DystoniaEdoardo Monfrini, Alessio Di Fonzo|Annals of Neurology|2021Cited by 28