DDOST Mutations Identified by Whole-Exome Sequencing Are Implicated in Congenital Disorders of Glycosylation

Melanie A. Jones; Bobby G. Ng; Shruti Bhide; Ephrem Chin; Devin Rhodenizer; Ping He; Marie-Estelle Losfeld; Miao He; Kimiyo Raymond; Gerard Berry; Hudson H. Freeze; Madhuri R. Hegde

doi:10.1016/j.ajhg.2011.12.024

DDOST Mutations Identified by Whole-Exome Sequencing Are Implicated in Congenital Disorders of Glycosylation

By Melanie A. Jones, Bobby G. Ng, Shruti Bhide, Ephrem Chin, Devin Rhodenizer, Ping He, Marie-Estelle Losfeld, Miao He, Kimiyo Raymond, Gerard Berry, Hudson H. Freeze and Madhuri R. Hegde

Publisher: Elsevier BV

Year: 2012

DOI identifier: 10.1016/j.ajhg.2011.12.024

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Provided by: MUCC (Crossref)

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DDOST Mutations Identified by Whole-Exome Sequencing Are Implicated in Congenital Disorders of Glycosylation

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