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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)

First Author: Eidhof I

Attributed to: MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

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