A Novel Mutation in MARS in a Patient with Charcot-Marie-Tooth Disease, Axonal, Type 2U with Congenital Onset

Charcot-Marie-Tooth disease is a phenotypically and genetically heterogeneous group of disorders affecting both motor and sensory neurons. Exome sequencing has driven discovery of genes responsible for Charcot-Marie-Tooth disease with more than 70 genes now associated with this neuromuscular disease...

Descripción completa

Detalles Bibliográficos
Autores principales: Gillespie, Meredith K., McMillan, Hugh J., Kernohan, Kristin D., Pena, Izabella A., Meyer-Schuman, Rebecca, Antonellis, Anthony, Boycott, Kym M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889022/
https://www.ncbi.nlm.nih.gov/pubmed/31356216
http://dx.doi.org/10.3233/JND-190404

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889022/
https://www.ncbi.nlm.nih.gov/pubmed/31356216
http://dx.doi.org/10.3233/JND-190404

Ejemplares similares