Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family
Research output: Contribution to journal › Journal article › Research › peer-review
| Original language | English |
|---|---|
| Journal | European Journal of Medical Genetics |
| Volume | 58 |
| Issue number | 12 |
| Pages (from-to) | 650-653 |
| Number of pages | 4 |
| ISSN | 1769-7212 |
| DOIs | |
| Publication status | Published - Dec 2015 |
- Deletions, 2p16.3 (NRXN1) deletion, 15q11.2 deletion, Schizophrenia, Family study, AK127244, Non-coding regions
Research areas
ID: 160893281