The genetics of Wilson disease
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Publisher
Elsevier
Reference141 articles.
1. Phenotypic and genetic characterization of a cohort of pediatric Wilson disease patients;Abdel Ghaffar;BMC Pediatr,2011
2. Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations;Abdelghaffar;J Hum Genet,2008
3. Update on Wilson disease;Aggarwal;Int Rev Neurobiol,2013
4. Wilson disease mutation pattern with genotype–phenotype correlations from Western India: confirmation of p.C271* as a common Indian mutation and identification of 14 novel mutations;Aggarwal;Ann Hum Genet,2013
5. A clinical and genetic study of 56 Saudi Wilson disease patients: identification of Saudi-specific mutations;Al Jumah;Eur J Neurol,2004
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1. Wilson Disease: Diagnostic Challenges and Differential Diagnoses;Clinical & Translational Metabolism;2024-07-26
2. Navigating the CRISPR/Cas Landscape for Enhanced Diagnosis and Treatment of Wilson’s Disease;Cells;2024-07-18
3. Wilson Disease: Copper-Mediated Cuproptosis, Iron-Related Ferroptosis, and Clinical Highlights, with Comprehensive and Critical Analysis Update;International Journal of Molecular Sciences;2024-04-26
4. The cost implications of Wilson disease among hospitalized patients: analysis of USA hospitals;European Journal of Gastroenterology & Hepatology;2024-04-23
5. The mutation spectrum and ethnic distribution of Wilson disease, a review;Molecular Genetics and Metabolism Reports;2024-03
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