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CMO I Deficiency Caused by a Point Mutation in Exon 8 of the HumanCYP11B2Gene Encoding Steroid 18-Hydroxylase (P450C18)
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1997
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Mendelian DisorderGenetic DisorderNatural SciencesGeneticsBiochemical GeneticsPoint MutationMolecular BiologyHumancyp11b2gene Encoding SteroidMolecular GeneticsGene ExpressionMedicineExon 8Mutagenesis
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