Hereditary tyrosinemia in Morocco: Clinical spectrum, diagnostic challenges, and genetic insights

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Authors: Samira Najeh, Miloud Hammoud, Es‐Said Sabir, Imane Assiri, Maroua Jakani, Abdelaati Berrachid, Sana El Foutat, Karima Lafha, Abdelkader Outzourhit, Naı̈ma Fdil
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Fields of Study & Subjects

Metabolism and Genetic Disorders Amino Acid Enzymes and Metabolism Genomics and Rare Diseases

Publication details

Journal / source
Molecular Genetics and Metabolism
Volume
147
Issue
2
Pages
109559–109559
Publication date
1 February 2026
Language
EN