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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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Detalhes bibliográficos
Main Authors: Scuderi, Soraya, La Cognata, Valentina, Drago, Filippo, Cavallaro, Sebastiano, D'Agata, Velia
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2014
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Acesso em linha: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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