Associated Papers
Phenotype and molecular characterization of Wilson's disease in Morocco.
Abbassi N et al.
Clinics and Research in Hepatology and Gastroenterology, 2024
Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients.
Lafhal K et al.
Molecular Genetics and Metabolism Reports, 2023
Characterization of mutation spectrum and identification of novel mutations in ATP7B gene from a cohort of Wilson disease patients: Functional and therapeutic implications.
Kumari N et al.
Human Mutation, 2018
Wilson's Disease and Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome in a Child: A Case Report with Lessons Learned!
Fernando M et al.
Euroasian Journal of Hepato-gastroenterology, 0
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