Linked Life Data

3502692

Source:http://linkedlifedata.com/resource/pubmed/id/3502692

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1987-6-8
pubmed:abstractText
A new variant of blood group A [A(WAS)] was expressed in three generations of a Caucasian family: Phenotype included weak mixed field hemagglutination by anti-A reagents, secretion of H substance, and presence of anti-A1 in serum. The A(WAS) variant was inherited in a Mendelian fashion, dominant to O. A-transferase activity was absent from cells and saliva but was 0.2% of normal A1 transferase activity in serum, with a pH optimum of 6.0. Family members expressing A(WAS) also demonstrated partly deficient H type on cells (Hm). H-transferase activity in serum was normal for a weak A subgroup and showed typical Km and acceptor specificities. Linkage of H-modifier and ABO loci cannot be excluded.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0009-9163
pubmed:author
pubmed:issnType
Print
pubmed:volume
31
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7-12
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1987
pubmed:articleTitle
"Unclassifiable" weak A blood group and deficient H phenotype (Hm) in one pedigree. Variants of A and H types in a family.
pubmed:publicationType
Journal Article, Case Reports