Novel insight into FCSK-congenital disorder of glycosylation through a CRISPR-generated cell model

CONCLUSION: 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.PMID:38722107 | PMC:PMC11080630 | DOI:10.1002/mgg3.2445

Source: Molecular Medicine - May 9, 2024 Category: Molecular Biology Authors: Maryam Fazelzadeh Haghighi Hossein Jafari Khamirani Jafar Fallahi Ali Arabi Monfared Korosh Ashrafi Dehkordi Seyed Mohammad Bagher Tabei Source Type: research