C. Lücking

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations

N. Quinn, P. Praamstra, M. Horstink, 2001, Neurology.

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

Y. Agid, A. Dürr, A. Brice, 1998, The Lancet.

Alpha-synuclein and Parkinson's disease

A. Brice, C. Lücking, C. Lücking, 2000, Cellular and Molecular Life Sciences CMLS.

Association between early-onset Parkinson's disease and mutations in the parkin gene.

Bonifati, N W Wood, A Dürr, 2000, The New England journal of medicine.

Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

A. Brice, M. Periquet, G. Meco, 2001, Neurology.

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

A. Destée, M. Farrer, S. Lincoln, 2003, Neurology.