| Original language | English |
|---|---|
| Pages (from-to) | 346-348 |
| Number of pages | 3 |
| Journal | Atherosclerosis |
| Volume | 206 |
| Issue number | 2 |
| DOIs | |
| State | Published - Oct 2009 |
Bibliographical note
Funding Information:This work was supported by a grant from the Catholic University Research Foundation made in the program year of 2008 (2008-A0016-00067) and a Korea Science and Engineering Foundation (KOSEF) grant funded by the Korea government (MOST) (No.R01-2006-000-10208-0).
Keywords
- Compound heterozygous mutation
- Familial LCAT deficiency
- High-density lipoprotein
- LCAT gene mutation