A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign.
| Image |  |
|---|---|
| Description | scientific article published on 14 June 2019 |
| Author/s |
author: Antonio Novelli Viola Alesi |
| Publication date | June 14, 2019 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |