Source:http://linkedlifedata.com/resource/pubmed/id/18028269
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
2008-1-30
|
| pubmed:abstractText |
The Kidd blood group antigens Jka and Jkb are encoded by the red blood cell (RBC) urea transporter gene. Homozygosity for silent JK alleles results in the rare Jk(a-b-) phenotype. To date, seven JKnull alleles have been identified, and of these, two are more frequent in the Polynesians and Finns. This study reports the identification of other JKnull alleles in Jk(a-b-) individuals of different ethnic or geographic origins.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0041-1132
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
48
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
365-72
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| pubmed:meshHeading |
pubmed-meshheading:18028269-Alleles,
pubmed-meshheading:18028269-Base Sequence,
pubmed-meshheading:18028269-Erythroid Cells,
pubmed-meshheading:18028269-Genome, Human,
pubmed-meshheading:18028269-Humans,
pubmed-meshheading:18028269-Introns,
pubmed-meshheading:18028269-Kidd Blood-Group System,
pubmed-meshheading:18028269-Membrane Transport Proteins,
pubmed-meshheading:18028269-Mutation
|
| pubmed:year |
2008
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| pubmed:articleTitle |
Erythroid urea transporter deficiency due to novel JKnull alleles.
|
| pubmed:affiliation |
Department of Laboratory Medicine, Division of Hematology and Transfusion Medicine, Lund University and Blood Center, University Hospital, Lund, Sweden.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|