Reply: A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia; and Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar ataxia-27 (SCAR27) in a Chinese family

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Publication year
2020
Author(s)
Eidhof, I.J.M.
Baets, J.
Kamsteeg, E.J.
Schenck, A.
Warrenburg, B.P.C. van de
Source
Brain, 143, 6, (2020), article e51
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DOI
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/2066/220470   https://hdl.handle.net/2066/220470
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