Authors:
Lucking, CB
Durr, A
Bonifati, V
Vaughan, J
De Michele, G
Gasser, T
Harhangi, BS
Meco, G
Denefle, P
Wood, NW
Agid, Y
Brice, A
Citation: Cb. Lucking et al., Association between early-onset Parkinson's disease and mutations in the parkin gene, N ENG J MED, 342(21), 2000, pp. 1560-1567
Authors:
Abbas, N
Lucking, CB
Ricard, S
Durr, A
Bonifati, V
De Michele, G
Bouley, S
Vaughan, JR
Gasser, T
Marconi, R
Broussolle, E
Brefel-Courbon, C
Harhangi, BS
Oostra, AB
Fabrizio, E
Bohme, GA
Pradier, L
Wood, NW
Filla, A
Meco, G
Denefle, P
Agid, Y
Brice, A
Citation: N. Abbas et al., A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe, HUM MOL GEN, 8(4), 1999, pp. 567-574
Authors:
Harhangi, BS
Farrer, MJ
Lincoln, S
Bonifati, V
Meco, G
De Michele, G
Brice, A
Durr, A
Martinez, M
Gasser, T
Bereznai, B
Vaughan, JR
Wood, NW
Hardy, J
Oostra, BA
Breteler, MMB
Citation: Bs. Harhangi et al., The lle93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease, NEUROSCI L, 270(1), 1999, pp. 1-4