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Genetic Modifiers and Non-Mendelian Aspects of CMT
Charcot-Marie-Tooth (CMT) neuropathies are amongst the most common inherited diseases in neurology. While great strides have been made to identify the genesis of these diseases, a diagnostic gap of 30–60% remains. Classic models of genetic causation may be limited to fully close this gap and, thus,...
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| Publicado no: | Brain Res |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6925904/ https://ncbi.nlm.nih.gov/pubmed/31525351 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2019.146459 |
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