<i>N</i>‐glycome analysis detects dysglycosylation missed by conventional methods in <scp>SLC39A8</scp> deficiency
Julien H. Park(University of Münster), Thorsten Marquardt(Klinik und Poliklinik für Kinder- und Jugendmedizin)
Cited by 19
Related Papers
Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn
|European Journal of Human Genetics|2012|39
Expanding the phenotypic spectrum of ARCN1-related syndrome
|Genetics in Medicine|2022|15
Ascorbate mitigates oxidative stress and hemin cytotoxicity in heme oxygenase-1 deficiency
|Journal of Biological Chemistry|2025|2