11961233

Source:http://linkedlifedata.com/resource/pubmed/id/11961233

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0078140, umls-concept:C0427620, umls-concept:C1314792, umls-concept:C1412099, umls-concept:C1708726, umls-concept:C1762617
pubmed:issue	3
pubmed:dateCreated	2002-4-18
pubmed:abstractText	A number of alleles have been described for ABO encoding for common and rare ABO blood group phenotypes. Critical mutations in the coding sequence of ABO that may confer the different specificity and activity of the glycosyltransferases encoded by this gene locus have been identified.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0417360
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ABO Blood-Group System, http://linkedlifedata.com/resource/pubmed/chemical/Arginine, http://linkedlifedata.com/resource/pubmed/chemical/Glycine
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0041-1132
pubmed:author	pubmed-author:BlasczykRainerR, pubmed-author:Eiz-VesperBrittaB, pubmed-author:HallenslebenMichaelM, pubmed-author:HeymannGiudoG, pubmed-author:LenhardVolkerV, pubmed-author:SeltsamAxelA
pubmed:issnType	Print
pubmed:volume	42
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	294-301
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:11961233-ABO Blood-Group System, pubmed-meshheading:11961233-Alleles, pubmed-meshheading:11961233-Arginine, pubmed-meshheading:11961233-Base Sequence, pubmed-meshheading:11961233-Blood Grouping and Crossmatching, pubmed-meshheading:11961233-Bosnia-Herzegovina, pubmed-meshheading:11961233-Erythrocytes, pubmed-meshheading:11961233-Exons, pubmed-meshheading:11961233-Germany, pubmed-meshheading:11961233-Glycine, pubmed-meshheading:11961233-Humans, pubmed-meshheading:11961233-Introns, pubmed-meshheading:11961233-Phenotype, pubmed-meshheading:11961233-Point Mutation, pubmed-meshheading:11961233-Polymerase Chain Reaction, pubmed-meshheading:11961233-Polymorphism, Genetic, pubmed-meshheading:11961233-Sequence Alignment, pubmed-meshheading:11961233-Sequence Analysis, DNA, pubmed-meshheading:11961233-Turkey
pubmed:year	2002
pubmed:articleTitle	A weak blood group A phenotype caused by a new mutation at the ABO locus.
pubmed:affiliation	Department of Transfusion Medicine, Hannover Medical School, Hannover, Germany.
pubmed:publicationType	Journal Article