المؤلفون: Laura Russo Zillmer, Marc Miravitlles, Leandro Genehr Fritscher, Heicilainy Del Carlos Gondim, Ivan Ivanaga, José Roberto Jardim, Altay Alves Lino de Souza, Rodrigo Russo, Beatriz Martins Manzano, Maria da Penha Uchoa Sales, Fernando Luiz Cavalcanti Lundgren, Maria Vera Cruz de Oliveira, Marcela Amorim Alves, Oliver A. Nascimento, Gildo Santos Jr

المصدر: Jornal Brasileiro de Pneumologia
Jornal Brasileiro de Pneumologia v.42 n.5 2016
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Volume: 42, Issue: 5, Pages: 311-316, Published: OCT 2016
Jornal Brasileiro de Pneumologia, Vol 42, Iss 5, Pp 311-316

مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Male, congenital, hereditary, and neonatal diseases and abnormalities, Genotype, alpha 1-antitrypsin deficiency/epidemiology, Doença pulmonar obstrutiva crônica/epidemiologia, Pulmonary disease, 03 medical and health sciences, Pulmonary Disease, Chronic Obstructive, 0302 clinical medicine, Gene Frequency, alpha 1-Antitrypsin Deficiency, Prevalence, Medicine, Alfa 1 antitripsina, Humans, In patient, 030212 general & internal medicine, Alleles, Aged, lcsh:RC705-779, alfa 1-antitripsina, business.industry, lcsh:Diseases of the respiratory system, Sequence Analysis, DNA, Middle Aged, Molecular biology, Deficiência de alfa 1-antitripsina/epidemiologia, Cross-Sectional Studies, 030228 respiratory system, Multicenter study, alpha 1-Antitrypsin, Female, Original Article, business, Alelos, Brazil, alpha 1-antitrypsin, pulmonary disease, chronic obstructive/epidemiology

وصف الملف: text/html

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a943dec46b3cdf5fe4a34bd47962f234
https://pubmed.ncbi.nlm.nih.gov/27812629