Sensory motor ataxic neuropathy associated dysarthria and ophthalmoplegia “SMANDO” in a consanguineous Moroccan patient with new POLG gene homozygote mutation
| Autor: | Rafai, M.A. *, Khattab, H., Jardel, C., Slassi, I., Dehbi, H., Bouche, P. |
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| Zdroj: | In Revue Neurologique January-February 2021 177(1-2):144-146 |
| Databáze: | ScienceDirect |
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