Senataxin gene mutation presenting with ataxia oculomotor apraxia type 2: Five patients with three different mutations
| Autor: | Seçil, Y., Subasioglu, A., Uzunkopru, C., Tanrıverdi, Z. |
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| Zdroj: | In Parkinsonism and Related Disorders October 2020 79 Supplement 1:e112-e112 |
| Databáze: | ScienceDirect |
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