Phenotypic and genetic characterization of children with Wilson Disease from Northeast China
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1186/s12887-024-05045-x.pdf
Reference37 articles.
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2. Kenney SM, Cox DW. Sequence variation database for the Wilson disease copper transporter, ATP7B. Hum Mutat. 2007;28:1171–7.
3. European Association for Study of Liver. EASL Clinical Practice guidelines: Wilson’s disease. J Hepatol. 2012;56(3):671–85.
4. Roberts EA, Schilsky ML, American Association for Study of Liver Diseases (AASLD). Diagnosis and treatment of Wilson disease: an update. Hepatology. 2008;47(6):2089–111.
5. Wiernicka A, Dądalski M, Jańczyk W, Kamińska D, Naorniakowska M, et al. Early Onset of Wilson Disease: Diagnostic challenges. J Pediatr Gastroenterol Nutr. 2017;65(5):555–60.
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