Exome Sequencing Reveals Immune Genes as Susceptibility Modifiers in Individuals with α(1)-Antitrypsin Deficiency

Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder associated to early onset emphysema, mainly imputable to Pi*ZZ genotype. In spite of the serious potential effects, many AATD individuals do not develop emphysema. To identify genes/variants potentially involved in emphysema development we...

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發表在:Sci Rep
Main Authors: Rigobello, Chiara, Baraldo, Simonetta, Tinè, Mariaenrica, Ferrarotti, Ilaria, Corsico, Angelo Guido, Bazzan, Erica, Turato, Graziella, Balestro, Elisabetta, Biondini, Davide, Valle, Giorgio, Saetta, Marina, Cosio, Manuel G.
格式: Artigo
語言:Inglês
出版: Nature Publishing Group UK 2019
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Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6739380/
https://ncbi.nlm.nih.gov/pubmed/31511551
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-49409-1
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