Phenotypic Heterogeneity in a Congenital Disorder of Glycosylation Caused by Mutations in STT3A

J Child Neurol. 2017 May;32(6):560-565. DOI:10.1177/0883073817696816. Epub 2017 Mar 16.

Ghosh A, Urquhart J, Daly S, Ferguson A, Scotcher D, Morris AAM, Clayton-Smith J

https://www.ncbi.nlm.nih.gov/pubmed/28424003

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