Succinyl-CoA:3-ketoacid transferase (SCOT) deficiency in a new patient homozygous for an R217X mutation. [electronic resource]

By: Contributor(s): Producer: 20050324Description: 691-2 p. digitalISSN:
  • 0141-8955
Subject(s): Online resources: In: Journal of inherited metabolic disease vol. 27
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Publication Type: Case Reports; Journal Article

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