Aasly, J.

patient mutation lrrk 2 disease 2019ser idiopathic pd symptom parkinson idiopathic deficiency neurology university muscle study lrrk 2-associated pd family onset centre frequency carrier haemolytic anaemia department hospital estimate phosphoglycerate research group penetrance consortium stage qsbb series kinase cause lrrk 2 mutations series pgk deficiency institute 10 years fference scale haemolytic london analysis prevalence control 79 years anaemia exercise disorder parkinsonism ffected grant table 2-associated method activity treatment glycogenosi population tremor article pd onset 69 years duration testing disease duration di fference dystonia myoglobinuria health progression incidence symptom onset individual genetic non-motor symptoms foundation state 40 years 59 years