Publication | Open Access
Multiple Sulfatase Deficiency Is Caused by Mutations in the Gene Encoding the Human Cα-Formylglycine Generating Enzyme
387
Citations
45
References
2003
Year
BiosynthesisBiochemistryGenetic DisorderNatural SciencesGeneticsBiochemical GeneticsMolecular BiologyProtein GeneticsGene EncodingMetabolismMedicineHuman Metabolism
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