A PRIMPOL mutation and variants in multiple genes may contribute to phenotypes in a familial case with chronic progressive external ophthalmoplegia symptoms
| Autor: | Kasamo, Kei, Nakamura, Masayuki ⁎, Daimou, Yoko, Sano, Akira |
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| Zdroj: | In Neuroscience Research August 2020 157:58-63 |
| Databáze: | ScienceDirect |
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