Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleCase Report: A rare form of congenital erythrocytosis due to SLC30A10 biallelic variants--differential diagnosis and recommendation for biochemical and genetic screening.AuthorsGiannini, Rosalinda; Agolini, Emanuele; Palumbo, Giuseppe; Novelli, Antonio; Garone, Giacomo; Grasso, Melissa; Colafati, Giovanna Stefania; Matraxia, Marta; Piccirilli, Eleonora; Deodati, Annalisa; Ceglie, GiuliaPublicationFrontiers in Pediatrics, 2024, p1ISSN2296-2360Publication typeArticleDOI10.3389/fped.2024.1319885