18338170

Source:http://linkedlifedata.com/resource/pubmed/id/18338170

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002892, umls-concept:C0003765, umls-concept:C0015127, umls-concept:C0021918, umls-concept:C0026882, umls-concept:C0035820, umls-concept:C0042845, umls-concept:C0061472, umls-concept:C0205251, umls-concept:C0220839, umls-concept:C1314792
pubmed:issue	7
pubmed:dateCreated	2008-5-23
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9107334
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Intrinsic Factor, http://linkedlifedata.com/resource/pubmed/chemical/Vitamin B 12
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1432-0584
pubmed:author	pubmed-author:BaigetMM, pubmed-author:CanalsCC, pubmed-author:Del RíoEE, pubmed-author:RIVAP CPC, pubmed-author:RemachaA FAF, pubmed-author:SardàM PMP
pubmed:issnType	Electronic
pubmed:volume	87
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	599-600
pubmed:meshHeading	pubmed-meshheading:18338170-Adult, pubmed-meshheading:18338170-Amino Acid Substitution, pubmed-meshheading:18338170-Anemia, Pernicious, pubmed-meshheading:18338170-Gastric Mucosa, pubmed-meshheading:18338170-Genetic Predisposition to Disease, pubmed-meshheading:18338170-Genotype, pubmed-meshheading:18338170-Humans, pubmed-meshheading:18338170-Intestinal Absorption, pubmed-meshheading:18338170-Intrinsic Factor, pubmed-meshheading:18338170-Mutation, Missense, pubmed-meshheading:18338170-Point Mutation, pubmed-meshheading:18338170-Risk, pubmed-meshheading:18338170-Vitamin B 12, pubmed-meshheading:18338170-Vitamin B 12 Deficiency
pubmed:year	2008
pubmed:articleTitle	Role of (Glu --> Arg, Q5R) mutation of the intrinsic factor in pernicious anemia and other causes of low vitamin B12.
pubmed:publicationType	Letter