Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s.
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| Title: | Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s. |
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| Authors: | Ueda M; University of Pennsylvania, Philadelphia, Pennsylvania (M.U.)., Burke FM; University of Pennsylvania Health System, Philadelphia, Pennsylvania (F.M.B.)., Remaley AT; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland (A.T.R.)., Hegele RA; Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada (R.A.H.)., Rader DJ; University of Pennsylvania and University of Pennsylvania Health System, Philadelphia, Pennsylvania (D.J.R.)., Dunbar RL; University of Pennsylvania and Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania (R.L.D.). |
| Source: | Annals of internal medicine [Ann Intern Med] 2020 Apr 07; Vol. 172 (7), pp. 500-502. Date of Electronic Publication: 2019 Nov 19. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: American College of Physicians--American Society of Internal Medicine Country of Publication: United States NLM ID: 0372351 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1539-3704 (Electronic) Linking ISSN: 00034819 NLM ISO Abbreviation: Ann Intern Med Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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