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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Veröffentlicht in:Allergy Asthma Immunol Res
Hauptverfasser: Vishweswaraiah, Sangeetha, Veerappa, Avinash M, Mahesh, Padukudru A, Jahromi, Sareh R, Ramachandra, Nallur B.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 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
Online Zugang: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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