bibliographic entry 2350235 [be/2350235]
https://w3id.org/oc/corpus/be/2350235

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  • Casals, F, Hodgkinson, A, Hussin, J, Idaghdour, Y, Bruat, V, de Maillard, T. Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans, PLoS Genet, 2013, 9, e1003815, DOI: 10.1371/journal.pgen.1003815, PMID: 24086152
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