Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights

Conclusions Here, using a structured approach, we have characterised a clinically and genetically well-defined dystonia cohort from Turkey, where dystonia has not been widely studied, and provided an uncovered genetic basis, which will facilitate diagnostic dystonia research.

http://jmg.bmj.com/cgi/content/short/61/5/443?rss=1

Source: Journal of Medical Genetics - April 19, 2024 Category: Genetics & Stem Cells Authors: Atasu, B., Simon-Sanchez, J., Hanagasi, H., Bilgic, B., Hauser, A.-K., Guven, G., Heutink, P., Gasser, T., Lohmann, E. Tags: Open access Neurogenetics Source Type: research