alg13造句

• ALG13 and ALG14 ( this protein ) constitute the UDP-GlcNAc transferase, which catalyzes a key step in endoplasmic reticulum N-linked glycosylation.
• Progress in genome and exome sequencing is revealing that some individuals diagnosed with Lennox Gastaut Syndrome have de novo mutations in a variety of genes, including CHD2, GABRB3, ALG13 and SCN2A The Epi4K study consortium ( 2013 ) observed de novo mutations in at least 15 % of a study cohort of 165 patients with LGS and Infantile Spasms using whole exome sequencing.