NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect

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Publication year
2018
Author(s)
Bartling, F.
Sanchez Caballero, L.M.
Brand, M.A.M. van den
Fung, C.W.
Chan, S.H.
Wong, V.C.
Hellebrekers, D.M.E.
Coo, I.F.M. de
Smeitink, J.A.M.
Rodenburg, R.J.T.
Nijtmans, L.G.J.
Source
Clinical Genetics, 93, 1, (2018), pp. 111-118
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/190456   https://hdl.handle.net/2066/190456
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