Two novel frame shift mutations in lecithin:cholesterol acyltransferase (LCAT) gene associated with a familial LCAT deficiency phenotype

Research output: Contribution to journalLetterpeer-review

5 Scopus citations
Original languageEnglish
Pages (from-to)346-348
Number of pages3
JournalAtherosclerosis
Volume206
Issue number2
DOIs
StatePublished - 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

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