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Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype.

Pubmed ID: 10384394 RIS Download

Mesh terms: Aspartic Acid | Child | Glycine | Humans | Infant | Membrane Proteins | Microbodies | Mutation | Peroxisomal Disorders | Phenotype | Zellweger Syndrome

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