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Kelch Domain of Gigaxonin Interacts with Intermediate Filament Proteins Affected in Giant Axonal Neuropathy

Patients with giant axonal neuropathy (GAN) show progressive loss of motor and sensory function starting in childhood and typically live for less than 30 years. GAN is caused by autosomal recessive mutations leading to low levels of gigaxonin (GIG), a ubiquitously-expressed BTB/Kelch cytoplasmic pro...

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Bibliografische gegevens
Gepubliceerd in:PLoS One
Hoofdauteurs: Johnson-Kerner, Bethany L., Garcia Diaz, Alejandro, Ekins, Sean, Wichterle, Hynek
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Public Library of Science 2015
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4604155/
https://ncbi.nlm.nih.gov/pubmed/26460568
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0140157
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