A case report of two Moroccan patients with hereditary neurological disorders and molecular modeling study on the S72L de novo PMP22 variant
| Autor: | Ait El Cadi, C., Dafrallah, L., Amalou, G., Charif, M., Charoute, H., Araqi-Houssaini, A., Lakhiari, H., Lenaers, G., Barakat, A. |
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| Zdroj: | In Revue Neurologique October 2023 179(8):902-909 |
| Databáze: | ScienceDirect |
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