Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy

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Publication year
2018
Author(s)
Wesdorp, F.M.
Schreur, V.
Beynon, A.J.
Oostrik, J.
Kamp, J.M. van de
Elting, M.
Feenstra, I.
Admiraal, R.J.C.
Kunst, H.P.M.
Hoyng, C.B.
Kremer, H.
Yntema, H.G.
Pennings, R.J.E.
Schraders, M.
Source
Clinical Genetics, 94, 2, (2018), pp. 221-231
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/194367   https://hdl.handle.net/2066/194367
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