Novel insight into FCSK-congenital disorder of glycosylation through a CRISPR-generated cell model.
Maryam Fazelzadeh HaghighiHossein Jafari KhamiraniJafar FallahiAli Arabi MonfaredKorosh Ashrafi DehkordiSeyed Mohammad Bagher TabeiPublished in: Molecular genetics & genomic medicine (2024)
This study expands insight into the FCSK-CDG molecular mechanism; to the best of our knowledge, it is the first research conducted to reveal a gene whose expression level alters due to this disease.