A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation
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| Description | article |
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author: Undiagnosed Diseases Network Ellen Macnamara David Parry Giedre Grigelioniene |
| Publication date | October 1, 2018 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |