Wilson Disease in Children
Author:
Publisher
Elsevier BV
Subject
Hepatology
Reference63 articles.
1. Tanner S: A History of Wilson Disease. In: Kerkar N, Roberts EA, eds Clinical and Translational Perspectives on Wilson Disease, Elsevier Publications: Academic press; London (UK): 2019; 1-11.
2. The Human Gene Mutation Database (HGMD) and its exploitation in the fields of personalized genomics and molecular evolution;Stenson;Curr Protoc Bioinformatics,2012
3. Wilson's disease;Ala;Lancet,2007
4. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene;Bull;Nat Genet,1993
5. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene;Petrukhin;Nat Genet,1993
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3. Wilson’s Disease Caused by Previously Undescribed Homozygous Nucleotide Variant of the <i>ATP7B</i> Gene: Clinical Cases;Current Pediatrics;2024-05-05
4. Disorders of Copper Metabolism in Children—A Problem too Rarely Recognized;Metabolites;2024-01-07
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