Variants in the genes DCTN2,DNAH10,LRIG3, and MYO1A are associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family

INTRODUCTION: Charcot–Marie–Tooth disease (CMT) is a heterogeneous inherited neuropathy. The number of known CMT genes is rapidly increasing mainly due to next‐generation sequencing technology, at present more than 70 CMT‐associated genes are known. We investigated whether variants in the DCTN2 coul...

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Detalles Bibliográficos
Autores principales: Braathen, G. J., Høyer, H., Busk, Ø. L., Tveten, K., Skjelbred, C. F., Russell, M. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057358/
https://www.ncbi.nlm.nih.gov/pubmed/26517670
http://dx.doi.org/10.1111/ane.12515

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057358/
https://www.ncbi.nlm.nih.gov/pubmed/26517670
http://dx.doi.org/10.1111/ane.12515

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