Abstract
More than 27,000 human genes have been sequenced and described. Only a few of these genes are relevant for common human diseases with regard to diagnostic or therapeutic purposes. This review describes the genetics of common traits and diseases with a particular focus on perspectives for drug discovery and drug therapy in neonates.
| Original language | English |
|---|---|
| Journal | Neonatology |
| Volume | 113 |
| Issue number | 4 |
| Pages (from-to) | 400-405 |
| Number of pages | 6 |
| ISSN | 1661-7800 |
| DOIs | |
| Publication status | Published - 01.05.2018 |
Funding
We thank all participating patients, parents, and physicians. This study was funded by the German Federal Ministry of Education and Research (GNN; BMBF 01ER0805 and BMBF 01ER1501).
