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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Ann Neurol
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: 2014
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars