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Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9. (2024)

First Author: Quinlivan R

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2023.11.012

PubMed Identifier: 38150892

Publication URI: http://europepmc.org/abstract/MED/38150892

Type: Journal Article/Review

Volume: 34

Parent Publication: Neuromuscular disorders : NMD

ISSN: 0960-8966