Novel Population Specific Autosomal Copy Number Variation and Its Functional Analysis amongst Negritos from Peninsular Malaysia

Copy number variation (CNV) has been recognized as a major contributor to human genome diversity. It plays an important role in determining phenotypes and has been associated with a number of common and complex diseases. However CNV data from diverse populations is still limited. Here we report the...

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Detalles Bibliográficos
Autores principales: Mokhtar, Siti Shuhada, Marshall, Christian R., Phipps, Maude E., Thiruvahindrapuram, Bhooma, Lionel, Anath C., Scherer, Stephen W., Peng, Hoh Boon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067311/
https://www.ncbi.nlm.nih.gov/pubmed/24956385
http://dx.doi.org/10.1371/journal.pone.0100371

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067311/
https://www.ncbi.nlm.nih.gov/pubmed/24956385
http://dx.doi.org/10.1371/journal.pone.0100371

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