| Property | Value |
|---|
| Working Groups |  Winkelmann |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  32366965 |
| DOI |  10.1038/s41436-020-0815-4 |
| Publication Year | 2020 |
| Title | De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy.  |
| Journal | Genetics in medicine : official journal of the American College of Medical Genetics |
| ISSN | 1098-3600 |
| ESSN | 1530-0366 |
| URL | https://www.ncbi.nlm.nih.gov/pubmed/?term=32366965%5Buid%5D |
| Pages | 1413-1417 |
| Issue | 8 |
| Volume | 22 |
| Journal Abbreviation | Genet Med |
| Authors | Singh S, Gupta A, Zech M, Sigafoos AN, Clark KJ, Dincer Y, Wagner M, Humberson JB, Green S, van Gassen K, Brandt T, Schnur RE, Millan F, Si Y, Mall V, Winkelmann J, Gavrilova RH, Klee EW, Engleman K, Safina NP, Slaugh R, Bryant EM, Tan WH, Granadillo J, Misra SN, Schaefer GB, Towner S, Brilstra EH, Koeleman BPC |
| First Author | Singh S |
| Last Author | Koeleman BPC |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
Q94521636https://www.wikidata.org/wiki/Q94521636
Wikidata ID
