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Unmasking a Case of Asymptomatic Charcot-Marie-Tooth Disease (CMT1A) With Vincristine
Charcot-Marie-Tooth (CMT) disease is a hereditary demyelinating disease of the peripheral nervous system that results in sensory and motor dysfunction. CMT includes a spectrum of diseases with different types of mutations in the genes encoding myelin protein, resulting in a variety of dysfunctions i...
Autores principales: | Jariwal, Roopam, Shoua, Basel, Sabetian, Katayoun, Natarajan, Piruthiviraj, Cobos, Everardo |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833168/ https://www.ncbi.nlm.nih.gov/pubmed/29511693 http://dx.doi.org/10.1177/2324709618758349 |
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