Author:
Minamizuka Takuya,Kobayashi Junji,Tada Hayato,Koshizaka Masaya,Maezawa Yoshiro,Yokote Koutaro
Funder
Ministry of Education, Culture, Sports, Science and Technology
Subject
Clinical Biochemistry,General Medicine
Reference14 articles.
1. J.R. Burnett, A. J. Hooper, R.A. Hegele, Familial Lipoprotein Lipase Deficiency. 1999 Oct 12 [updated 2017 Jun 22]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022.
2. Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene;Benlian;N. Engl. J. Med.,1996
3. Novel LPL mutation (L303F) found in a patient associated with coronary artery disease and severe systemic atherosclerosis;Saika;Eur. J. Clin. Invest.,2003
4. No evidence of accelerated atherosclerosis in a 66-yr-old chylomicronemia patient homozygous for the nonsense mutation (Tyr61–>stop) in the lipoprotein lipase gene;Ebara;Atherosclerosis.,2001
5. A 60-y-old chylomicronemia patient homozygous for missense mutation (G188E) in the lipoprotein lipase gene showed no accelerated atherosclerosis;Ebara;Clin. Chim. Acta.,2007
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