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Charcot-Marie-Tooth disease with pyramidal features due to a new mutation of EGR2 gene
Background and aim of the work: Childhood-onset peripheral neuropathies are often of genetic origin. Charcot-Marie-Tooth (CMT), is considered the commonest neuromuscular disorder. Due to its high clinical heterogeneity, especially in the pediatric age, the co-existence of central and peripheral symp...
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| Publicat a: | Acta Biomed |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Mattioli 1885
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6502152/ https://ncbi.nlm.nih.gov/pubmed/30889162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.23750/abm.v90i1.6951 |
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