Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation

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Publication year
1996
Author(s)
Coo, I.F.M. de
Smeets, H.J.M.
Gabreëls, F.J.M.
Arts, N.J.M.
Oost, B.A. van
Source
American Journal of Human Genetics, 58, 3, (1996), pp. 636-638
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Publication type
Article / Letter to editor
If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/24194   https://hdl.handle.net/2066/24194
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