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
Open Access
- 18 May 2020
- journal article
- letter
- Published by Oxford University Press (OUP) in Brain
- Vol. 143 (6), e51
- https://doi.org/10.1093/brain/awaa122
Abstract
No abstract availableFunding Information
- E-RARE-3 Joint Transnational Call
- ZonMw (9003037604)
- Association Belge contre les Maladies Neuromusculaires (EU FP7/2007-2013, 2012-305121)
- Senior Clinical Researcher mandate of the Research Fund - Flanders
- ZonMw
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