Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

Authors

Gustav Schonfeld, Washington University School of Medicine in St. Louis
Pin Yue, Washington University School of Medicine in St. Louis
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Journal

The New England Journal of Medicine

Publication Date

2010

Volume

363

Issue

23

Inclusive Pages

2220-2227

Document Type

Open Access Publication

DOI

pdf/10.1056/NEJMoa1002926

Rights and Permissions

Musunuru, K., Pirruccello, J. P., Do, R., Peloso, G. M., Guiducci, C., Sougnez, C., . . . Kathiresan, S. (2010). Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia. New England Journal of Medicine, 363(23), 2220-2227. Copyright © 2010 Massachusetts Medical Society. doi: 10.1056/NEJMoa1002926. http://www.nejm.org/doi/pdf/10.1056/NEJMoa1002926.

Recommended Citation

Schonfeld, Gustav; Yue, Pin; and et al, "Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia." The New England Journal of Medicine. 363, 23. 2220-2227. (2010).
https://digitalcommons.wustl.edu/open_access_pubs/3065