|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0002085,
umls-concept:C0031437,
umls-concept:C0078140,
umls-concept:C0205314,
umls-concept:C0206243,
umls-concept:C0332281,
umls-concept:C0679622,
umls-concept:C1412099,
umls-concept:C1442161,
umls-concept:C1555721,
umls-concept:C1706204,
umls-concept:C1762617
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|
pubmed:issue |
7
|
|
pubmed:dateCreated |
2010-7-19
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|
pubmed:abstractText |
The 1061delC single-nucleotide polymorphism (SNP) has been reported mostly in the context of the common A(2)[A201] allele and typically produces an A(2) phenotype. This study evaluated new A(weak) alleles, each containing 1061delC.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jul
|
|
pubmed:issn |
1537-2995
|
|
pubmed:author |
|
|
pubmed:issnType |
Electronic
|
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pubmed:volume |
50
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1471-86
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pubmed:meshHeading |
pubmed-meshheading:20456702-ABO Blood-Group System,
pubmed-meshheading:20456702-Alleles,
pubmed-meshheading:20456702-Amino Acid Substitution,
pubmed-meshheading:20456702-Flow Cytometry,
pubmed-meshheading:20456702-Gene Deletion,
pubmed-meshheading:20456702-Humans,
pubmed-meshheading:20456702-Models, Molecular,
pubmed-meshheading:20456702-Mutation, Missense,
pubmed-meshheading:20456702-Phenotype,
pubmed-meshheading:20456702-Polymorphism, Single Nucleotide
|
|
pubmed:year |
2010
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|
pubmed:articleTitle |
Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.
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|
pubmed:affiliation |
Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
