Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns-Reference-Cited by-同舟云学术

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Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns

Published:2012 Issue:1 Volume:7 Page:56
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

Tanner Stephan M,Sturm Amy C,Baack Elizabeth C,Liyanarachchi Sandya,de la Chapelle Albert

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Cited by 49 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Imerslund-Gräsbeck syndrome: a comprehensive review of reported cases;Orphanet Journal of Rare Diseases;2023-09-14

3. Fatty acids, selenium, and vitamin B12 in chub mackerel (Scomber colias) as nourishment considering seasonality and bioaccessibility as factors;Food Chemistry;2023-03

4. The complex machinery of human cobalamin metabolism;Journal of Inherited Metabolic Disease;2023-02-08

5. Síndrome de Imerslund-Gränsbeck: revisión sistemática de casos clínicos;CES Medicina;2022-11-16

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