Associated Papers
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies.
Schröter J et al.
European Journal of Human Genetics : Ejhg, 2022
Tubulin mutations in neurodevelopmental disorders as a tool to decipher microtubule function.
Fourel G et al.
Febs Letters, 2020
Extragenic suppression of motA missense mutations of Escherichia coli.
Garza AG et al.
Journal of Bacteriology, 1996
Select a paper to view details