A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes
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Dustin N. Hartzel | D. Rader | M. Ritchie | S. Damrauer | R. Judy | M. Levin | R. Kember | Joseph Park | C. Haggerty | D. Hartzel | N. Reza | A. Owens
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