| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2839544 | Clínica e Investigación en Arteriosclerosis | 2015 | 7 Pages |
Abstract
Our results suggest that LMF1 mutations are involved in a substantial proportion of cases with severe HTG, putting together the moderate-aggressive effect of rare mutations with polymorphisms classically associated with this disease.
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Authors
Itziar Lamiquiz-Moneo, Ana M. Bea, RocÃo Mateo-Gallego, LucÃa Baila-Rueda, Ana Cenarro, Miguel PocovÃ, Fernando Civeira, Isabel de Castro-Orós,