Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-41022-6.pdf
Reference50 articles.
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3. Lim, E. T. et al. Distribution and medical impact of loss-of-function variants in the Finnish founder population. PLoS genetics 10, e1004494, https://doi.org/10.1371/journal.pgen.1004494 (2014).
4. Casals, F. et al. Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. PLoS genetics 9, e1003815, https://doi.org/10.1371/journal.pgen.1003815 (2013).
5. Tang, D. et al. Reference genotype and exome data from an Australian Aboriginal population for health-based research. Sci Data 3, 160023, https://doi.org/10.1038/sdata.2016.23 (2016).
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