Associated Papers
Imerslund-Gräsbeck syndrome: a comprehensive review of reported cases.
Kingma SDK et al.
Orphanet Journal of Rare Diseases, 2023
37710296 (PubMed )
Supplement: 13023_2023_2889_MOESM2_ESM.xlsx › Tabel_artikel
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
Tanner SM et al.
Orphanet Journal of Rare Diseases, 2012
Imerslund-Gräsbeck syndrome: new mutation in amnionless.
Densupsoontorn N et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2012
Select a paper to view details