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Three novel mutations, c314C>A, C778insC, and c1285+2T>A, in exon 2 of the Wilson disease gene
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2000
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Mendelian DisorderDisease MechanismGenetic DisorderWilson Disease GeneGeneticsNovel MutationsMolecular BiologyPathologyMolecular GeneticsDisease Gene IdentificationGenomicsMedicineExon 2
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