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Article

Canine Imerslund-Gräsbeck syndrome maps to a region orthologous to HSA14q.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Nov 2003

He Qianchuan, Fyfe John C, Schäffer Alejandro A, Kilkenney Adam, Werner Petra, Kirkness Ewen F, Henthorn Paula S

Abstract excerpt

Selective malabsorption of cobalamin (vitamin B(12)) accompanied by proteinuria, known as Imerslund-Gräsbeck syndrome or megaloblastic anemia 1 (I-GS, MGA1; OMIM 261100), is a rare autosomal recessive disorder. In Finnish kindreds, I-GS is caused by mutations in the cubilin gene ( CUBN), located...

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Source

Identifiers

PMID: 14722725
DOI: 10.1007/s00335-003-2280-1

Genes

AMN
CUBN
EML1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-14722725-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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