Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. (2020)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41588-020-0649-7

PubMed Identifier: 32457452

Publication URI: http://europepmc.org/abstract/MED/32457452

Type: Journal Article/Review

Volume: 52

Parent Publication: Nature genetics

Issue: 6

ISSN: 1061-4036