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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Detalles Bibliográficos
Autores principales: Vishweswaraiah, Sangeetha, Veerappa, Avinash M, Mahesh, Padukudru A, Jahromi, Sareh R, Ramachandra, Nallur B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397367/
https://www.ncbi.nlm.nih.gov/pubmed/25749760
http://dx.doi.org/10.4168/aair.2015.7.3.265

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397367/
https://www.ncbi.nlm.nih.gov/pubmed/25749760
http://dx.doi.org/10.4168/aair.2015.7.3.265

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