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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
1999-11-18
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pubmed:abstractText |
Severe alpha-1-antitrypsin (ATT) deficiency is an inherited disorder associated with a high risk of developing pulmonary emphysema and several liver diseases. Over 90 different variants of gene which expresses AAT have been described. The commonest defective variants are Z and S. Determination of gene frequencies of abnormal variants is important to estimate the number of subjects at risk of suffering from diseases related with severe AAT deficiency in any given population.
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pubmed:language |
spa
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0025-7753
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:day |
2
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pubmed:volume |
113
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
366-70
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10562938-Adolescent,
pubmed-meshheading:10562938-Adult,
pubmed-meshheading:10562938-Aged,
pubmed-meshheading:10562938-Aged, 80 and over,
pubmed-meshheading:10562938-Alleles,
pubmed-meshheading:10562938-Child,
pubmed-meshheading:10562938-Child, Preschool,
pubmed-meshheading:10562938-Female,
pubmed-meshheading:10562938-Genotype,
pubmed-meshheading:10562938-Humans,
pubmed-meshheading:10562938-Male,
pubmed-meshheading:10562938-Middle Aged,
pubmed-meshheading:10562938-Phenotype,
pubmed-meshheading:10562938-Spain,
pubmed-meshheading:10562938-alpha 1-Antitrypsin
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pubmed:year |
1999
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pubmed:articleTitle |
[Allelic frequency of the gene of alpha-1-antitrypsin in the general population in a county in Asturias].
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pubmed:affiliation |
Sección de Neumología, Hospital Valle del Nalón, Asturias. hunv@hvn.org
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pubmed:publicationType |
Journal Article,
English Abstract
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