COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
- Heeringa, S.F.
- Chernin, G.
- Chaki, M.
- Zhou, W.
- Sloan, A.J.
- Ji, Z.
- Xie, L.X.
- Salviati, L.
- Hurd, T.W.
- Vega-Warner, V.
- Killen, P.D.
- Raphael, Y.
- Ashraf, S.
- Ovunc, B.
- Schoeb, D.S.
- McLaughlin, H.M.
- Airik, R.
- Vlangos, C.N.
- Gbadegesin, R.
- Hinkes, B.
- Saisawat, P.
- Trevisson, E.
- Doimo, M.
- Casarin, A.
- Pertegato, V.
- Giorgi, G.
- Prokisch, H.
- Rötig, A.
- Nürnberg, G.
- Becker, C.
- Wang, S.
- Ozaltin, F.
- Topaloglu, R.
- Bakkaloglu, A.
- Bakkaloglu, S.A.
- Müller, D.
- Beissert, A.
- Mir, S.
- Berdeli, A.
- Özen, S.
- Zenker, M.
- Matejas, V.
- Santos-Ocaña, C.
- Navas, P.
- Kusakabe, T.
- Kispert, A.
- Akman, S.
- Soliman, N.A.
- Krick, S.
- Mundel, P.
- Reiser, J.
- Nürnberg, P.
- Clarke, C.F.
- Wiggins, R.C.
- Faul, C.
- Hildebrandt, F.
- Show all authors +
ISSN: 0021-9738, 1558-8238
Year of publication: 2011
Volume: 121
Issue: 5
Pages: 2013-2024
Type: Article