Biochemical and Hematologic Manifestations of Gastric Intrinsic Factor (GIF) Deficiency: A Treatable Cause of B12 Deficiency in the Old Order Mennonite Population of Southwestern Ontario-Reference-Cited by-同舟云学术

Biochemical and Hematologic Manifestations of Gastric Intrinsic Factor (GIF) Deficiency: A Treatable Cause of B12 Deficiency in the Old Order Mennonite Population of Southwestern Ontario

Published:2014 Issue: Volume: Page:69-77
ISSN:2192-8304
Container-title:JIMD Reports
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Author:

Ferrand A.,Siu V. M.,Rupar C. A.,Napier M. P.,Al-Dirbashi O. Y.,Chakraborty P.,Prasad C.

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/8904_2014_351

Reference20 articles.

1. Ament AE, Li Z, Sturm AC et al (2009) Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF. Br J Haematol 144(4):622–624

2. Boina Abdallah A, Ogier de Baulny H, Kozyraki R et al (2012) How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B(12) absorption? Mol Genet Metab 107(1–2):66–71

3. Carmel R, Green R, Rosenblatt DS, Watkins D (2003) Update on cobalamin, folate, and homocysteine. Hematology Am Soc Hematol Educ Program 62–81

4. Chery C, Hehn A, Mrabet N et al (2013) Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant. Biochimie 95(5):995–1001

5. Garcia Jimenez MC, Baldellou Vazquez A, Calvo Martin MT, Perez-Lungmus G, Lopez Pison J (2008) Hereditary juvenile cobalamin deficiency due to mutations in GIF gene. Anales de Pediatria (Barcelona, Spain: 2003) 69(1):56–58

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