Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype. [electronic resource]

By: Contributor(s): Producer: 19990910Description: 311-3 p. digitalISSN:
  • 0141-8955
Subject(s): Online resources: In: Journal of inherited metabolic disease vol. 22
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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