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We present a patient with microcephaly, dysmorphic facies, congenital heart defect, focal epilepsy, infantile spasms, skeletal dysplasia, and a type 1 serum transferrin isoelectrofocusing due to a novel CDG caused by a homozygous variant in the oligosaccharyltransferase complex noncatalytic subunit (<jats:italic>OSTC<\/jats:italic>) gene involved in glycosylation and confirmed by serum transferrin electrophoresis.<\/jats:p>","DOI":"10.1002\/ajmg.a.61553","type":"journal-article","created":{"date-parts":[[2020,4,8]],"date-time":"2020-04-08T11:26:05Z","timestamp":1586345165000},"page":"1460-1465","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["Oligosaccharyltransferase complex\u2010congenital disorders of glycosylation: A novel congenital disorder of glycosylation"],"prefix":"10.1002","volume":"182","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5393-6687","authenticated-orcid":false,"given":"Emily M.","family":"Bryant","sequence":"first","affiliation":[{"name":"Ann &amp; Robert H. 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