Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia

RATIONALE: Bronchopulmonary dysplasia is the most common chronic respiratory disease in premature infants. Genetic factors might contribute to bronchopulmonary dysplasia susceptibility. OBJECTIVES: To identify genetic variants involved in bronchopulmonary dysplasia through a genome-wide association...

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Publicado en:Am J Respir Crit Care Med
Autores principales: Hadchouel, Alice, Durrmeyer, Xavier, Bouzigon, Emmanuelle, Incitti, Roberto, Huusko, Johanna, Jarreau, Pierre-Henri, Lenclen, Richard, Demenais, Florence, Franco-Montoya, Marie-Laure, Layouni, Ines, Patkai, Juliana, Bourbon, Jacques, Hallman, Mikko, Danan, Claude, Delacourt, Christophe
Formato: Artigo
Lenguaje:Inglês
Publicado: American Thoracic Society 2011
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4826668/
https://ncbi.nlm.nih.gov/pubmed/21836138
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201103-0548OC
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