Associated Papers
Imerslund-Gräsbeck syndrome in a child with a novel compound heterozygous mutations in the AMN gene: a case report.
Zhang D et al.
Italian Journal of Pediatrics, 2024
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
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