Charles Explorer logo
🇨🇿

Central European Group on Genetics of Movement Disorders

Publikace na 1. lékařská fakulta, 2. lékařská fakulta |
2023

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

Over the last two decades, we have witnessed major developments in neurogenetic research, the aetiopathogenesis and possible treatment options. Although substantial progress has been made, the first genome-wide studies have explained relatively little of the heritability of most complex traits, leading to a theory that a more fine-scale analysis considering the characteristics of individual populations may hold the key to the missing heritability.