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Analysis of the T1288R Mutation of the Wilson Disease ATP7B Gene in Four Generations of a Family: Possible Genotype-Phenotype Correlation with Hepatic Onset

Mendelian DisorderHepatologyGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyT1288r MutationMolecular BiologyPathologyFour GenerationsMolecular GeneticsDisease Gene IdentificationGenomicsPossible Genotype-phenotype CorrelationMedicine