Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy.
| Image |  |
|---|---|
| Description | scientific article published on 26 March 2016 |
| Author/s | |
| Publication date | March 26, 2016 |
| Language | English |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |