COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

1. Heeringa, S.F.
2. Chernin, G.
3. Chaki, M.
4. Zhou, W.
5. Sloan, A.J.
6. Ji, Z.
7. Xie, L.X.
8. Salviati, L.
9. Hurd, T.W.
10. Vega-Warner, V.
11. Killen, P.D.
12. Raphael, Y.
13. Ashraf, S.
14. Ovunc, B.
15. Schoeb, D.S.
16. McLaughlin, H.M.
17. Airik, R.
18. Vlangos, C.N.
19. Gbadegesin, R.
20. Hinkes, B.
21. Saisawat, P.
22. Trevisson, E.
23. Doimo, M.
24. Casarin, A.
25. Pertegato, V.
26. Giorgi, G.
27. Prokisch, H.
28. Rötig, A.
29. Nürnberg, G.
30. Becker, C.
31. Wang, S.
32. Ozaltin, F.
33. Topaloglu, R.
34. Bakkaloglu, A.
35. Bakkaloglu, S.A.
36. Müller, D.
37. Beissert, A.
38. Mir, S.
39. Berdeli, A.
40. Özen, S.
41. Zenker, M.
42. Matejas, V.
43. Santos-Ocaña, C.
44. Navas, P.
45. Kusakabe, T.
46. Kispert, A.
47. Akman, S.
48. Soliman, N.A.
49. Krick, S.
50. Mundel, P.
51. Reiser, J.
52. Nürnberg, P.
53. Clarke, C.F.
54. Wiggins, R.C.
55. Faul, C.
56. Hildebrandt, F.
57. Show all authors +

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DOI: 10.1172/JCI45693 GOOGLE SCHOLAR lock_openOpen access editor

Data source: Scopus