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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Publicado en:Allergy Asthma Immunol Res
Autores principales: Vishweswaraiah, Sangeetha, Veerappa, Avinash M, Mahesh, Padukudru A, Jahromi, Sareh R, Ramachandra, Nallur B.
Formato: Artigo
Lenguaje:Inglês
Publicado: 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
Acceso en línea: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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