Novel ndufa13 mutations associated with oxphos deficiency and leigh syndrome: A second family report

1. González-Quintana, A.
2. García-Consuegra, I.
3. Belanger-Quintana, A.
4. Serrano-Lorenzo, P.
5. Lucia, A.
6. Blázquez, A.
7. Docampo, J.
8. Ugalde, C.
9. Morán, M.
10. Arenas, J.
11. Martín, M.A.

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DOI: 10.3390/GENES11080855 GOOGLE SCHOLAR lock_openOpen access editor

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