A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency

Published 2013 View Full Article

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Title
A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency
Authors
Keywords
Missense Mutation, TCEP, Uncharged Amino Acid, Swiss Light Source, Ketone Body Utilization
Journal
JOURNAL OF INHERITED METABOLIC DISEASE
Volume 36, Issue 6, Pages 983-987
Publisher
Springer Nature
Online
2013-02-19
DOI
10.1007/s10545-013-9589-z
References
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