About: Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles

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About: Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles Goto Sponge NotDistinct Permalink

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scientific article published on 16 November 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 2007 (uk) article scientifique publié en 2007 (fr) im November 2007 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 16 November 2007 (en) artículu científicu espublizáu en payares de 2007 (ast)
publication date	wds:Q79909628-E651E783-0F3F-47E3-B0B0-23CA0FAA235F
publication date	2007-11-16 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q79909628-BDAA8004-B41A-4A30-9231-2300D4C390E8
language of work or name	English
author name string	wds:Q79909628-318DB571-65D3-4DCF-9D86-210ECC960A25 wds:Q79909628-353F57FF-17A8-4B30-9F97-02BDC2268ADC wds:Q79909628-BD0CEEBE-4E83-43BC-B642-5B252A3F25DB wds:Q79909628-BE240F23-617B-46CF-AD06-9EFC0BAD25FC
author name string	Jos P M Wielders Rob J Kraaijenhagen Brenda B van der Meijden Janke Prins
rdfs:label	Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles (en) Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles (nl)
skos:prefLabel	Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles (en) Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles (nl)
name	Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles (en) Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles (nl)
title	wds:Q79909628-E6D8E67F-F65E-42A6-8812-D409D0E6A2DE
title	Inherited chronic obstructive pulmonary disease: new selective-sequencing workup for alpha1-antitrypsin deficiency identifies 2 previously unidentified null alleles (en)
page(s)	wds:Q79909628-BF11B83C-AECD-462D-9FA4-C7A7A1E8296C
page(s)	101-107
instance of	wds:Q79909628-08E12A41-6587-4504-9E61-1963ADA22E00
instance of	scholarly article
main subject	wds:Q79909628-0A081E07-20A2-425E-8548-7E828E62D537
main subject	chronic obstructive pulmonary disease
PubMed ID	wds:Q79909628-C2D0228F-0DD3-4BBC-A901-F9297C85224B
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18024524
PubMed ID	18024524
published in	wds:Q79909628-C55D2435-68B8-4AAE-A056-6CB00F61DEF0
published in	Clinical Chemistry
issue	wds:Q79909628-2B06C30A-FBB1-4607-8C68-35CB27D3FC32
volume	wds:Q79909628-A407C0DE-F6FC-4FA7-8E14-AEF0C3BC3B6C
issue	1
volume	54
DOI	wds:Q79909628-932D8D7A-5A89-4196-9EED-1B89E663BF62
DOI	http://dx.doi.org/10.1373/CLINCHEM.2007.095125
DOI	10.1373/CLINCHEM.2007.095125
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q79909628
is cites work of	Severe alpha-1 antitrypsin deficiency in composite heterozygotes inheriting a new splicing mutation QOMadrid Clinical heterogeneity and potential high pathogenicity of the Mmalton Alpha 1 antitrypsin allele at the homozygous, compound heterozygous and heterozygous states C reactive protein and alpha1-antitrypsin: relationship between levels and gene variants Identification and characterisation of eight novel SERPINA1 Null mutations Identification of a novel SERPINA-1 mutation causing alpha-1 antitrypsin deficiency in a patient with severe bronchiectasis and pulmonary embolism Screening for Alpha 1 antitrypsin deficiency in Tunisian subjects with obstructive lung disease: a feasibility report. Alpha1-antitrypsin deficiency: a clinical-genetic overview Is an integrative laboratory algorithm more effective in detecting alpha-1-antitrypsin deficiency in patients with premature chronic obstructive pulmonary disease than AAT concentration based screening approach?
is cites work of	wds:Q36131624-BAD52E23-EC7F-4C75-98D5-A34D2A239D88 wds:Q84112341-46820D11-22CA-4908-976A-A452BC1DF0D0 wds:Q33852125-B30F3A05-C790-445E-85D8-E0C8202A712E wds:Q36925199-8542A4D0-6C50-40EF-8E23-D786B7FF4AE6 wds:Q34325994-13CA0411-79D4-421B-975F-FC58A2E23F62 wds:Q35596461-BE6BFF11-268A-4573-BDCB-8218946A34BA wds:Q34630059-7F06F81A-5BCE-4B4E-BF5A-87A51D50B96D wds:Q37166417-E01B08D6-157E-4A94-88D3-91E07D9EC07A

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