539P A late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition is more common in West of Scotland than primary genetic MADD, and is likely multifactorial
Year: 2024
Type: article
Source: Neuromuscular Disorders
Authors: T. Watson-Fargie, A. Coomber, M. Barr, K. Brennan, J. Dale, E. Fletcher, P. Gallagher, E. Molinari, E. Miller-Hodges, D. O'Sullivan, K. Stewart, R. Taylor, A. Topf, V. Straub, R. Edwards, W. Stewart, M. Farrugia, C. Longman
Language: English
Subfield: Clinical Biochemistry
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4403138687