Alpha-1 Antitrypsin PiMZ Genotype Is Associated with Chronic Obstructive Pulmonary Disease in Two Racial Groups
about
Diagnosing alpha-1 antitrypsin deficiency: the first step in precision medicine.A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants.Genome-wide association study of lung function and clinical implication in heavy smokers
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Alpha-1 Antitrypsin PiMZ Genotype Is Associated with Chronic Obstructive Pulmonary Disease in Two Racial Groups
description
article
@en
im August 2017 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована в серпні 2017
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name
Alpha-1 Antitrypsin PiMZ Genot ...... y Disease in Two Racial Groups
@en
Alpha-1 Antitrypsin PiMZ Genot ...... y Disease in Two Racial Groups
@nl
type
label
Alpha-1 Antitrypsin PiMZ Genot ...... y Disease in Two Racial Groups
@en
Alpha-1 Antitrypsin PiMZ Genot ...... y Disease in Two Racial Groups
@nl
prefLabel
Alpha-1 Antitrypsin PiMZ Genot ...... y Disease in Two Racial Groups
@en
Alpha-1 Antitrypsin PiMZ Genot ...... y Disease in Two Racial Groups
@nl
P2093
P2860
P1476
Alpha-1 Antitrypsin PiMZ Genot ...... y Disease in Two Racial Groups
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P2093
Carla Wilson
Craig P Hersh
Dawn L DeMeo
Edwin K Silverman
Farshid N Rouhani
Gerard Criner
James D Crapo
John E Hokanson
John Ziniti
Marilyn G Foreman
P2860
P304
P356
10.1513/ANNALSATS.201611-838OC
P407
P577
2017-08-01T00:00:00Z