𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson’s disease

✍ Scribed by Elisabeth Leroy; Dimitri Anastasopoulos; Spiridon Konitsiotis; Christian Lavedan; M. H. Polymeropoulos

Publisher
Springer
Year
1998
Tongue
English
Weight
100 KB
Volume
103
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A consanguineous Turkish family with ear
A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion
✍ Okan Dogu; Janel Johnson; Dena Hernandez; Melissa Hanson; John Hardy; Hulya Apay 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 229 KB

## Abstract The importance of parkin in early‐onset Parkinson's disease in Japan, Europe, and the United States is well established. The contribution of this gene to the risk of Parkinson's disease in other populations is less well known. To explore the importance of parkin in those of Turkish ance

Deletion of the parkin and PACRG gene pr
Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism
✍ Suzanne Lesage; Periquet Magali; Ebba Lohmann; Lucette Lacomblez; Helio Teive; S 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 210 KB 👁 1 views

## Communicated by Christine Van Broeckhoven Autosomal recessive mutations in the parkin gene (PARK2) have been identified as a common cause of familial and also sporadic, early-onset parkinsonism (EOPD): point mutations, exonic deletions, and duplications or triplications have been described. Her

Parkinson's disease in Ireland: Clinical
Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations
✍ Joseph Wiley; Timothy Lynch; Sarah Lincoln; Lisa Skipper; Mary Hulihan; David Go 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 71 KB

## Abstract Early‐onset autosomal recessive parkinsonism is associated with parkin gene mutations. Different parkin mutations occur in many ethnic backgrounds; however, the phenotype may vary. We studied 102 young‐onset (age at onset <60 years) Parkinson's disease (PD) patients. From 102 patients,