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. (2020)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awaa122
PubMed Identifier: 32428197
Publication URI: http://europepmc.org/abstract/MED/32428197
Type: Journal Article/Review
Volume: 143
Parent Publication: Brain : a journal of neurology
Issue: 6
ISSN: 0006-8950