Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference17 articles.
1. Very long-chain acyl-CoA dehydrogenase deficiency;Leslie,1993
2. Atypical presentation of VLCAD 147 deficiency associated with a novel ACADVL splicing mutation;Shchelochkov;Muscle Nerve,2009
3. Rhabdomyolysis in the military: recognizing late-onset very long-chain acyl Co-A dehydrogenase deficiency;Hoffman;Mil. Med.,2006
4. A primigravida with very-long chain acyl-CoA dehydrogenase deficiency;Murata;Muscle Nerve,2014
5. Very long chain acyl-CoA dehydrogenase deficiency in a pair of mildly affected monozygotic twin sister in their late fifties;Zia;J. Inherit. Metab. Dis.,2007
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