Congenital myasthenia and congenital disorders of glycosylation caused by mutations in the DPAGT1 gene
| Autor: | Ibáñez-Micó, S., Domingo Jiménez, R., Pérez-Cerdá, C., Ghandour-Fabre, D. |
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| Zdroj: | In Neurología (English Edition) March 2019 34(2):139-141 |
| Databáze: | ScienceDirect |
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