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High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations

(2011) HUMAN MUTATION. 32(11). p.1290-1298
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Keywords
CORONARY-ARTERY-DISEASE, APOLIPOPROTEIN-A-I, FISH EYE DISEASE, ACYLTRANSFERASE DEFICIENCY, STRUCTURE PREDICTION, FAMILIAL LECITHIN, PROTEIN-STRUCTURE, ATHEROSCLEROSIS, SERVER, hypoalphalipoproteinemia, HIGH-DENSITY-LIPOPROTEIN, familial LCAT deficiency, fish-eye disease

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Citation

Please use this url to cite or link to this publication:

Chicago
Holleboom, Adriaan G, Jan A Kuivenhoven, Frank Peelman, Alinda W Schimmel, Jorge Peter, Joep C Defesche, John JP Kastelein, G Kees Hovingh, Erik S Stroes, and Mohammad Mahdi Motazacker. 2011. “High Prevalence of Mutations in LCAT in Patients with Low HDL Cholesterol Levels in The Netherlands: Identification and Characterization of Eight Novel Mutations.” Human Mutation 32 (11): 1290–1298.
APA
Holleboom, A. G., Kuivenhoven, J. A., Peelman, F., Schimmel, A. W., Peter, J., Defesche, J. C., Kastelein, J. J., et al. (2011). High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations. HUMAN MUTATION, 32(11), 1290–1298.
Vancouver
1.
Holleboom AG, Kuivenhoven JA, Peelman F, Schimmel AW, Peter J, Defesche JC, et al. High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations. HUMAN MUTATION. 2011;32(11):1290–8.
MLA
Holleboom, Adriaan G, Jan A Kuivenhoven, Frank Peelman, et al. “High Prevalence of Mutations in LCAT in Patients with Low HDL Cholesterol Levels in The Netherlands: Identification and Characterization of Eight Novel Mutations.” HUMAN MUTATION 32.11 (2011): 1290–1298. Print.
@article{3128986,
  author       = {Holleboom, Adriaan G and Kuivenhoven, Jan A and Peelman, Frank and Schimmel, Alinda W and Peter, Jorge and Defesche, Joep C and Kastelein, John JP and Hovingh, G Kees and Stroes, Erik S and Motazacker, Mohammad Mahdi},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  language     = {eng},
  number       = {11},
  pages        = {1290--1298},
  title        = {High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in The Netherlands: identification and characterization of eight novel mutations},
  url          = {http://dx.doi.org/10.1002/humu.21578},
  volume       = {32},
  year         = {2011},
}

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