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Description
This disorder is caused by an inherited deficiency of glutaryl-CoA dehydrogenase, which is involved in the catabolic pathways of L-lysine, L-hydroxylysine and L-tryptophan (97)
PMID: 34 AttiaHFinocchiFOrcianiMMehdiMZidiIJrahLazzariniRet al
Rebecca K
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The sex-specific associations were mostly based on the UK Biobank, which also need replication in other data sources when available
