Ataxia, myoclonus, deafness, and neuropathy in a family carrying the mtDNA 11778/ND4 mutation previously associated with Leber's hereditary optic neuropathy
| Autor: | AMATI BONNEAU, P, Reynier, P, Iommarini, L, Valentino, Ml, LA MORGIA, C, Bellan, M, Dollfus, H, Moulignier, A, Ducos, G, Orssaud, C, Achilli, Alessandro, Olivieri, A, Pala, M, Torroni, A, Carelli, V. |
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| Jazyk: | angličtina |
| Rok vydání: | 2008 |
| Databáze: | OpenAIRE |
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