Novel compound heterozygous COG5 mutations in a Chinese male patient with severe clinical symptoms and type IIi congenital disorder of glycosylation: A case report.
Yin S, Gong L, Qiu H, Zhao Y, Zhang Y, Liu C, Jiang H, Mao Y, Kong LY, Liang B, et al. Exp Ther Med. 2019 Oct; 18(4):2695-2700. Epub 2019 Jul 30.