Abnormal neurofilament inclusions and segregations in dorsal root ganglia of a Charcot-Marie-Tooth type 2E mouse model

Charcot-Marie-Tooth (CMT) disease or hereditary motor and sensory neuropathy is the most prevalent inherited peripheral neuropathy and is associated with over 90 causative genes. Mutations in neurofilament light polypeptide gene, NEFL cause CMT2E, an axonal form of CMT that results in abnormal struc...

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Detalles Bibliográficos
Autores principales: Zhao, Jian, Brown, Kristy, Liem, Ronald K. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487060/
https://www.ncbi.nlm.nih.gov/pubmed/28654681
http://dx.doi.org/10.1371/journal.pone.0180038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487060/
https://www.ncbi.nlm.nih.gov/pubmed/28654681
http://dx.doi.org/10.1371/journal.pone.0180038

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