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This page is a summary of: A neonatal‐onset succinyl‐CoA:3‐ketoacid CoA transferase (SCOT)‐deficient patient with T435N and c.658‐666dupAACGTGATT p.N220_I222dup mutations in the OXCT1 gene, Journal of Inherited Metabolic Disease, July 2010, Wiley,
DOI: 10.1007/s10545-010-9168-5.
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