Sequencing of Charcot-Marie-Tooth disease genes in a toxic polyneuropathy

OBJECTIVE: Mutations in Charcot-Marie-Tooth disease (CMT) genes are the cause of rare familial forms of polyneuropathy. Whether allelic variability in CMT genes is also associated with common forms of polyneuropathy—considered “acquired” in medical parlance—is unknown. Chemotherapy induced periphera...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:Ann Neurol
Main Authors: Beutler, Andreas S., Kulkarni, Amit A., Kanwar, Rahul, Klein, Christopher J., Therneau, Terry M., Qin, Rui, Banck, Michaela S., Boora, Ganesh K., Ruddy, Kathryn J., Wu, Yanhong, Smalley, Regenia L., Cunningham, Julie M., Le-Lindqwister, Nguyet Anh, Beyerlein, Peter, Schroth, Gary P., Windebank, Anthony J., Züchner, Stephan, Loprinzi, Charles L.
Formato: Artigo
Idioma:Inglês
Publicado: 2014
Assuntos:
Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4388308/
https://ncbi.nlm.nih.gov/pubmed/25164601
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24265
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares