Usefulness of exome sequencing in the study of spastic paraparesis and cerebellar atrophy: de novo mutation of the KIF1A gene, a new hope in prognosis
| Autor: | Urtiaga Valle, S., Fournier Gil, B., Ramiro León, M.S., Martínez Menéndez, B. |
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| Zdroj: | In Neurología (English Edition) September 2020 35(7):535-538 |
| Databáze: | ScienceDirect |
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