Systematic Review and UK-Based Study ofPARK2 (parkin), PINK1, PARK7 (DJ-1)andLRRK2in early-onset Parkinson's disease

Frequency of Known Mutations in Early-Onset Parkinson Disease

(2010) Roy N. Alcalay et al.   ARCHIVES OF NEUROLOGY

Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

(2010) Coro Paisán-Ruiz et al.   MOVEMENT DISORDERS

The effect of onset age on the clinical features of Parkinson’s disease

(2009) M. M. Wickremaratchi et al.   EUROPEAN JOURNAL OF NEUROLOGY

Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control

(2009) J Brooks et al.   JOURNAL OF MEDICAL GENETICS

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

(2008) Jose Bras et al.   BMC Neurology

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

(2008) Daniel G Healy et al.   LANCET NEUROLOGY

Familial Parkinsonism with digenicparkinandPINK1mutations

(2008) Manabu Funayama et al.   MOVEMENT DISORDERS

MDPD: an integrated genetic information resource for Parkinson's disease

(2008) S. Tang et al.   NUCLEIC ACIDS RESEARCH