C. B. Lücking

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.

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.

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

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

The parkin gene and its phenotype

Y. Agid, R. Marconi, M. Breteler, 2001, Neurological Sciences.

Alpha-synuclein and Parkinson's disease

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

Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany

C. Gieger, T. Illig, M. Dichgans, 2010, Neurobiology of Aging.

Absence of the mitochondrial A7237T mutation in Parkinson's disease.

M. Graeber, S. Kösel, P. Mehraein, 1995, Biochemical and biophysical research communications.

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

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