Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene, GIF.

British journal of haematology - 1 Aug 2010

Overgaard Ulrik M, Tanner Stephan M, Birgens Henrik S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Mutation
Share to Vitamin B 12 Deficiency

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Open in PubMed Open full text

Identifiers

PMID: 20408840
DOI: 10.1111/j.1365-2141.2010.08198.x
PMCID: PMC2914612

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene, GIF.PMID 20408840Read ↗

Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF.Semantic proximity Read ↗

[Homozygous mutation in the intrinsic factor gene in a child with severe vitamin B12 deficiency].Semantic proximity Read ↗

Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.Semantic proximity Read ↗

Acute lymphoblastic leukemia and vitamin B12 deficiency secondary to a gastric intrinsic factor gene mutation.Semantic proximity Read ↗

Megalobastic anemia, infantile leukemia, and immunodeficiency caused by a novel homozygous mutation in the DHFR gene.Semantic proximity Read ↗

Sjögren-Larsson syndrome due to a novel mutation in the FALDH gene.Semantic proximity Read ↗

The idic(15) syndrome: expanding the phenotype.Semantic proximity Read ↗

Genetic Disorders and the Fetus. Diagnosis, Prevention and TreatmentSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.