Copy Number Variation Burden on Asthma Subgenome in Normal Cohorts Identifies Susceptibility Markers

PURPOSE: Asthma is a complex disease caused by interplay of genes and environment on the genome of an individual. Copy number variations (CNVs) are more common compared to the other variations that disrupt genome organization. The effect of CNVs on asthma subgenome has been less studied compared to...

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Detalhes bibliográficos
Publicado no:Allergy Asthma Immunol Res
Main Authors: Vishweswaraiah, Sangeetha, Veerappa, Avinash M, Mahesh, Padukudru A, Jahromi, Sareh R, Ramachandra, Nallur B.
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2015
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4397367/
https://ncbi.nlm.nih.gov/pubmed/25749760
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4168/aair.2015.7.3.265
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