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 |
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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 |