Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype

Abstract Background Congenital disorders of glycosylation (CDG) are a group of heterogeneous disorders caused by abnormal lipid or protein glycosylation. Variants in the FCSK gene have been reported to cause CDG. Defective FCSK‐induced CDG (FCSK–CDG) has only been reported previously in three unrela...

Ful tanımlama

Detaylı Bibliyografya
Asıl Yazarlar: Abeer Al Tuwaijri, Yusra Alyafee, Muhammad Umair, Arwa Alsubait, Mashael Alharbi, Hamad AlEidi, Mariam Ballow, Mohammed Aldrees, Qamre Alam, Abdulkareem Al Abdulrahman, Muhammad Talal Alrifai, Majid Alfadhel
Materyal Türü: Makale
Dil:English
Baskı/Yayın Bilgisi: Wiley 2023-04-01
Seri Bilgileri:Molecular Genetics & Genomic Medicine
Konular:
Online Erişim:https://doi.org/10.1002/mgg3.2117

Benzer Materyaller