Published in
Elsevier, Genetics in Medicine, 1(22), p. 102-111, 2020
DOI: 10.1038/s41436-019-0625-8
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A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes
Journal article published in 2020 by
Nosheen Reza 
,
Marylyn D. Ritchie,
Michael G. Levin ,
Daniel J. Rader ,
Christopher M. Haggerty ,
Dustin N. Hartzel,
Renae Judy,
Rachel L. Kember ,
Joseph Park ,
Anjali T. Owens,
Scott M. Damrauer
,
Marylyn D. Ritchie,
Michael G. Levin ,
Daniel J. Rader ,
Christopher M. Haggerty ,
Dustin N. Hartzel,
Renae Judy,
Rachel L. Kember ,
Joseph Park ,
Anjali T. Owens,
Scott M. Damrauer
This paper was not found in any repository, but could be made available legally by the author.
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