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10 ensaios clínicos encontrados.
A Rare Combination of Hereditary Folate Malabsorption (SLC46A1 Gene Variant) and Beta-Thalassemia Trait.
📖 RevisãoHereditary Folate Malabsorption Presenting With Pancytopenia in Two Siblings: A Case Report.
Mechanistic insights into mutation in the proton-coupled folate transporter (SLC46A1) causing hereditary folate malabsorption.
Hereditary Folate Malabsorption.
Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations.