Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation

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Publication year
2016
Author(s)
Hartmann, B.
Wai, T.
Hu, H
MacVicar, T.
Musante, L.
Fischer-Zirnsak, B.
Stenzel, W.
Gräf, R.
Heuvel, L.P.W.J. van den
Ropers, H.H.
Wienker, T.F.
Hübner, C.
Langer, T.
Kaindl, A.M.
Source
Elife, 6, 5, (2016), pp. pii: e16078, article pii: e16078
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DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/172690   https://hdl.handle.net/2066/172690
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