Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group

Lancet. 1998 Oct 24;352(9137):1355-6. doi: 10.1016/s0140-6736(05)60746-5.

Authors

C B Lücking, N Abbas, A Dürr, V Bonifati, A M Bonnet, T de Broucker, G De Michele, N W Wood, Y Agid, A Brice

PMID: 9802278
DOI: 10.1016/s0140-6736(05)60746-5

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Adult
Algeria
Child
Europe
Exons
Female
Gene Deletion*
Humans
Male
Middle Aged
Parkinson Disease / genetics*
Phenotype