2 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
| 1 | 16153625 | Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome. | 2006 Feb | 1 |
| 2 | 6328478 | Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII. | 1984 May | 2 |