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Reply: A homozygous GDAP2 loss-of-function variant in a pat..:
Eidhof, Ilse
;
Baets, Jonathan
;
Kamsteeg, Erik-Jan
..
Brain. 143 (2020) 6 - p. e51-e51 , 2020
Link:
https://doi.org/10.1093/brain/awaa122
RT Journal T1
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
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_brain_awaa122&Exemplar=1&LAN=DE A1 Eidhof, Ilse A1 Baets, Jonathan A1 Kamsteeg, Erik-Jan A1 Schenck, Annette A1 van de Warrenburg, Bart P PB Oxford University Press (OUP) YR 2020 SN 0006-8950 SN 1460-2156 JF Brain VO 143 IS 6 SP e51 OP e51 LK http://dx.doi.org/https://doi.org/10.1093/brain/awaa122 DO https://doi.org/10.1093/brain/awaa122 SF ELIB - SuUB Bremen
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