𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Analysis of the parkin deletion in sporadic and familial Parkinson's disease

✍ Scribed by R. Krüger; A. M. M. Vieira-Säcker; W. Kuhn; T. Müller; D. Woitalla; L. Schöls; H. Przuntek; J. T. Epplen; O. Riess


Publisher
Springer
Year
1999
Tongue
English
Weight
68 KB
Volume
106
Category
Article
ISSN
1435-1463

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


The role of parkin in familial and spora
✍ Ted M. Dawson; Valina L. Dawson 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 122 KB 👁 1 views

## Abstract Mutations in parkin are the second most common known cause of Parkinson's disease (PD). Parkin is an ubiquitin E3 ligase that monoubiquitinates and polyubiquitinates proteins to regulate a variety of cellular processes. Loss of parkin's E3 ligase activity is thought to play a pathogenic

Tyrosine hydroxylase polymorphism in fam
✍ V. Planté-Bordeneuve; M. B. Davis; D. M. Maraganore; C. D. Marsden; Professor A. 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 283 KB

## Abstract Tyrosine hydroxylase (TH) is a theoretical candidate gene determining susceptibility to Parkinson's disease (PD), and an association between one allele of a polymorphism at the TH locus and sporadic PD has been reported. We investigated TH polymorphism in 44 patients with sporadic PD, 4