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Molecular Pathogenesis of Wilson Disease Among Indians: A Perspective on Mutation Spectrum in ATP7B gene, Prevalent Defects, Clinical Heterogeneity and Implication Towards Diagnosis

Mendelian DisorderDisease MechanismMolecular PathogenesisGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseasePathologyAtp7b GeneMolecular GeneticsWilson DiseaseDisease Gene IdentificationGenomicsMedicineEpidemiologyClinical Genetics