A familial case of Leigh Disease related to NDUFV1 homozygous mutations
| Autor: | Acer, H., Canpolat, M., Özçora, G.K., Kumandaş, S. |
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| Zdroj: | In European Journal of Paediatric Neurology June 2017 21 Supplement 1:e133-e134 |
| Databáze: | ScienceDirect |
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