ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes
在患有神经发育障碍表型的个体中发现的UBA7基因变异会破坏ISGylation。
期刊:iScience
影响因子:4.1
doi:10.1016/j.isci.2026.115454
Bandi, Venkateshwarlu; Venema, Myrrhe; Wallace, Iona; Mol, Merel O; Nikoncuk, Anita; Schot, Rachel; van Slegtenhorst, Marjon; Bijlsma, Emilia K; Khan, Amjad; White, Susan M; Rius, Rocio; Delatycki, Martin B; Narayanan, Vinodh; Swatek, Kirby N; Barakat, Tahsin Stefan; Bustos, Francisco
