Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation

Autor: Thierry Hennet, Siegrun Schnabel, Patricie Paesold-Burda, Heinz Troxler, Matthias R. Baumgartner, Peter Kleinert, Charlotte Maag, François Foulquier

Publikováno v: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2009, epub ahead of print. ⟨10.1093/hmg/ddp389⟩
Human Molecular Genetics, 2009, epub ahead of print. ⟨10.1093/hmg/ddp389⟩

International audience; The conserved oligomeric Golgi (COG) complex is a tethering factor composed of eight subunits that is involved in the retrograde transport of intra-Golgi components. Deficient biosynthesis of COG subunits leads to alterations

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f780ae702c0f90c3c402548c3f287d6
https://doi.org/10.5167/uzh-25739