Author:
Himmelreich Nastassja,Dimitrov Bianca,Zielonka Matthias,Hüllen Andreas,Hoffmann Georg Friedrich,Juenger Hendrik,Müller Herbert,Lorenz Imke,Busse Birgit,Marschall Christoph,Schlüter Gregor,Thiel Christian
Funder
European Commission
Deutsche Forschungsgemeinschaft
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference25 articles.
1. A method and server for predicting damaging missense mutations
2. N-linked protein glycosylation in the ER;Aebi;Biochim. Biophys. Acta,2013
3. Congenital disorders of glycosylation: the Saudi experience;Alsubhi;Am. J. Med. Genet. A,2017
4. Synergistic use of glycomics and single-molecule molecular inversion probes (smMIPs) for IDENTIFICATION of congenital disorders of glycosylation type-1;Bakar;J. Inherit. Metab. Dis.,2022
5. ALG9 mutation carriers develop kidney and liver cysts;Besse;J. Am. Soc. Nephrol.,2019
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