Alternative Splicing Generates Different Parkin Protein Isoforms: Evidences in Human, Rat, and Mouse Brain

Parkinson protein 2, E3 ubiquitin protein ligase (PARK2) gene mutations are the most frequent causes of autosomal recessive early onset Parkinson's disease and juvenile Parkinson disease. Parkin deficiency has also been linked to other human pathologies, for example, sporadic Parkinson disease,...

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Hlavní autoři: Scuderi, Soraya, La Cognata, Valentina, Drago, Filippo, Cavallaro, Sebastiano, D'Agata, Velia
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi Publishing Corporation 2014
Témata:
Review Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4124806/
https://ncbi.nlm.nih.gov/pubmed/25136611
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/690796
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