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
oleh: S. Urtiaga Valle, B. Fournier Gil, M.S. Ramiro León, B. Martínez Menéndez
| Format: | Article |
|---|---|
| Diterbitkan: | Elsevier España 2020-09-01 |
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