Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism
- 1 October 1998
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 352 (9137) , 1355-1356
- https://doi.org/10.1016/s0140-6736(05)60746-5
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Autosomal Recessive Juvenile Parkinsonism Maps to 6q25.2-q27 in Four Ethnic Groups: Detailed Genetic Mapping of the Linked RegionAmerican Journal of Human Genetics, 1998
- Chromosome 6–Linked Autosomal Recessive Early-Onset Parkinsonism: Linkage in European and Algerian Families, Extension of the Clinical Spectrum, and Evidence of a Small Homozygous Deletion in One FamilyAmerican Journal of Human Genetics, 1998
- Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismNature, 1998
- Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonismNeurology, 1996