Giant axonal neuropathy–associated gigaxonin mutations impair intermediate filament protein degradation

Giant axonal neuropathy (GAN) is an early-onset neurological disorder caused by mutations in the GAN gene (encoding for gigaxonin), which is predicted to be an E3 ligase adaptor. In GAN, aggregates of intermediate filaments (IFs) represent the main pathological feature detected in neurons and other...

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Main Authors: Mahammad, Saleemulla, Murthy, S.N. Prasanna, Didonna, Alessandro, Grin, Boris, Israeli, Eitan, Perrot, Rodolphe, Bomont, Pascale, Julien, Jean-Pierre, Kuczmarski, Edward, Opal, Puneet, Goldman, Robert D.
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Clinical Investigation 2013
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3635735/
https://ncbi.nlm.nih.gov/pubmed/23585478
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI66387
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