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Identification of an A-to-G Missense Mutation in Exon 2 of the UGT1 Gene Complex That Causes Crigler-Najjar Syndrome Type 2
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1993
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A-to-g Missense MutationMendelian DisorderUgt1 Gene ComplexGenetic DisorderGeneticsPathologyGenetic MechanismMolecular GeneticsDisease Gene IdentificationGene ExpressionMedicineExon 2
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