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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1980-2-28
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pubmed:abstractText |
A genetic analysis of human urinary pepsinogen isozymes is presented. Nine discrete phenotypes were identified in a population survey of 215 unrelated Caucasian individuals. The phenotypes were characterized by differences among the staining intensities of the activated group I pepsinogens, Pg 5, Pg 4, Pg 3, and Pg 2. The genetic studies demonstrated that the codominant expression of four alleles, PgA, PgB, PgC and PgD, at a single genetic locus determined the nine phenotypes identified. Linkage analysis excluded close linkage of the Pg locus with the chromosome 6 markers HLA, GLO1, and Bf.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
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pubmed:issn |
0340-6717
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
52
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
227-38
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading | |
pubmed:year |
1979
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pubmed:articleTitle |
Urinary pepsinogen isozymes: a highly polymorphic locus in man.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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