Behr’s syndrome is typically associated with disturbed mitochondrial translation and mutations in the C12orf65 gene

1. Pyle, A.
2. Ramesh, V.
3. Bartsakoulia, M.
4. Boczonadi, V.
5. Gomez-Duran, A.
6. Herczegfalvi, A.
7. Blakely, E.L.
8. Smertenko, T.
9. Duff, J.
10. Eglon, G.
11. Moore, D.
12. Man, P.Y.W.
13. Douroudis, K.
14. Santibanez-Koref, M.
15. Griffin, H.
16. Lochmüller, H.
17. Karcagi, V.
18. Taylor, R.W.
19. Chinnery, P.F.
20. Horvath, R.

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DOI: 10.3233/JND-140003 GOOGLE SCHOLAR lock_openOpen access editor

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