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NRG2779
NRG2779
http://dx.doi.org/10.1038/NRG2779
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
P356
Q37755970-7ED50707-5F84-4548-8460-09844FB21EC9
P356
NRG2779
http://dx.doi.org/10.1038/NRG2779