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Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development
Much has been achieved in terms of understanding the complex clinical and genetic heterogeneity of Charcot-Marie-Tooth neuropathy (CMT). Since the identification of mutations in the first CMT associated gene, PMP22, the technological advancement in molecular genetics and gene technology has allowed...
Gorde:
| Argitaratua izan da: | J Neurol Neurosurg Psychiatry |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BMJ Publishing Group
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6327864/ https://ncbi.nlm.nih.gov/pubmed/30018047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp-2018-318834 |
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