Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT.
| Image |  |
|---|---|
| Description | scientific article published on 5 June 2013 |
| Author/s |
author: Nicholas Katsanis |
| Publication date | June 5, 2013 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |