|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
6
|
|
pubmed:dateCreated |
1996-11-1
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|
pubmed:abstractText |
Severe alpha-1-antitrypsin (AAT) deficiency is caused by homozygous inheritance of gene Z, and is associated with a high risk of developing pulmonary emphysema. Determination of frequencies of different genes associated with the deficiency (especially S and Z) gives a clue to estimate the number of individuals homozygous PiZZ, carrying a high risk for pulmonary disease, in any given population.
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pubmed:language |
spa
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jul
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|
pubmed:issn |
0025-7753
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:day |
6
|
|
pubmed:volume |
107
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
211-4
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|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8755448-Adolescent,
pubmed-meshheading:8755448-Adult,
pubmed-meshheading:8755448-Alleles,
pubmed-meshheading:8755448-Female,
pubmed-meshheading:8755448-France,
pubmed-meshheading:8755448-Gene Frequency,
pubmed-meshheading:8755448-Humans,
pubmed-meshheading:8755448-Italy,
pubmed-meshheading:8755448-Male,
pubmed-meshheading:8755448-Middle Aged,
pubmed-meshheading:8755448-Phenotype,
pubmed-meshheading:8755448-Portugal,
pubmed-meshheading:8755448-Spain,
pubmed-meshheading:8755448-United States,
pubmed-meshheading:8755448-alpha 1-Antitrypsin,
pubmed-meshheading:8755448-alpha 1-Antitrypsin Deficiency
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|
pubmed:year |
1996
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|
pubmed:articleTitle |
[Study of the frequency of different phenotypes of alpha-1-antitrypsin in a population of Barcelona].
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|
pubmed:affiliation |
Servei de Pneumologia, Hospital General Universitari de la Vall d'Hebron, Barcelona.
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pubmed:publicationType |
Journal Article,
Comparative Study,
English Abstract,
Research Support, Non-U.S. Gov't
|
