Xènia Ferrer-Cortès
2PUBLICATIONS
8CO-AUTHORS
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Publications (2)
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|Jul 31, 2024
Novel transferrin gene mutations in four new cases of congenital Atransferrinaemia: Functional and diagnostic pathogenicity despite negative bioinformatics.Lídia Romero-Cortadellas, Xènia Ferrer-Cortès, Laura Calvo-López
|Apr 23, 2022
New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation.Lídia Romero-Cortadellas, Gonzalo Hernández, Xènia Ferrer-Cortès
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Lídia Romero-Cortadellas
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Mayka Sánchez
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Gonzalo Hernández
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José Luis Fuster
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Ana María Galera-Miñarro
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Laura Calvo-López
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Cristina Diaz-de-Heredia
