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Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

✍ Scribed by CB Lücking; N Abbas; A Dürr; V Bonifati; A-M Bonnet; T de Broucker; G De Michele; NW Wood; Y Agid; A Brice


Book ID
117288526
Publisher
The Lancet
Year
1998
Tongue
English
Weight
94 KB
Volume
352
Category
Article
ISSN
0140-6736

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Mutation analysis of the parkin gene in
✍ Sergei N. Illarioshkin; Magali Periquet; Nina Rawal; Christoph B. Lücking; Tatya 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 833 KB

## Abstract Autosomal recessive juvenile parkinsonism (AR‐JP) is a form of hereditary parkinsonism characterized by variable clinical presentations and caused by mutations in a novel gene, __parkin__, on chromosome 6q25.2–27. Until now, no Russian cases of __parkin__‐associated AR‐JP have been repo