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Cited by in F6Publishing
For: Borgel A, Lamoril J, Tchernitchko D. Mutations and polymorphisms associated with iron overload in a series of 91 non-HFE haemochromatosis patients. Clin Res Hepatol Gastroenterol 2020;44:239-41. [PMID: 31640930 DOI: 10.1016/j.clinre.2019.09.007] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Baas FS, Rishi G, Swinkels DW, Subramaniam VN. Genetic Diagnosis in Hereditary Hemochromatosis: Discovering and Understanding the Biological Relevance of Variants. Clin Chem 2021;67:1324-41. [PMID: 34402502 DOI: 10.1093/clinchem/hvab130] [Reference Citation Analysis]
2 de Gennes C, Lamoril J, Borgel A, Boi C, Yao R, Boileau C, Tchernitchko D. Severe iron overload in a woman with homeostatic iron regulator (HFE) and a novel 5'-aminolevulinate synthase 2 (ALAS2) mutations: interactions of multiple genetic determinants. Br J Haematol 2021. [PMID: 34490613 DOI: 10.1111/bjh.17810] [Reference Citation Analysis]
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