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/s41588-020-0615-4

PubMed Identifier: 32367058

Publication URI: http://europepmc.org/abstract/MED/32367058

Type: Journal Article/Review

Volume: 52

Parent Publication: Nature genetics

Issue: 5

ISSN: 1061-4036