Mutations in STT3A and STT3B cause two congenital disorders of glycosylation.
Shrimal, Shiteshu; Ng, Bobby G.; Losfeld, Marie-Estelle; Gilmore, Reid; Freeze, Hudson H.; Human Molecular Genetics, 2013, vol. 22, issue 22, p 4638, ISSN 09646906. ISBN 14602083.

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