Microtubule-associated protein 1B: a neuronal binding partner for gigaxonin

Giant axonal neuropathy (GAN), an autosomal recessive disorder caused by mutations in GAN, is characterized cytopathologically by cytoskeletal abnormality. Based on its sequence, gigaxonin contains an NH(2)-terminal BTB domain followed by six kelch repeats, which are believed to be important for pro...

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Detalles Bibliográficos
Autores principales: Ding, Jianqing, Liu, Jia-Jia, Kowal, Anthony S., Nardine, Timothy, Bhattacharya, Priyanka, Lee, Arthur, Yang, Yanmin
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173828/
https://www.ncbi.nlm.nih.gov/pubmed/12147674
http://dx.doi.org/10.1083/jcb.200202055

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173828/
https://www.ncbi.nlm.nih.gov/pubmed/12147674
http://dx.doi.org/10.1083/jcb.200202055

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