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Mutations in the X-linked ATP6AP2 cause a glycosylation dis..:
Rujano, Maria A
;
Serio, Magda Cannata
;
Panasyuk, Ganna
...
qt8001g5w8. , 2017
Link:
https://escholarship.org/uc/item/8001g5w8
RT Journal T1
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt8001g5w8&Exemplar=1&LAN=DE A1 Rujano, Maria A A1 Serio, Magda Cannata A1 Panasyuk, Ganna A1 Péanne, Romain A1 Reunert, Janine A1 Rymen, Daisy A1 Hauser, Virginie A1 Park, Julien H A1 Freisinger, Peter A1 Souche, Erika A1 Guida, Maria Clara A1 Maier, Esther M A1 Wada, Yoshinao A1 Jäger, Stefanie A1 Krogan, Nevan J A1 Kretz, Oliver A1 Nobre, Susana A1 Garcia, Paula A1 Quelhas, Dulce A1 Bird, Thomas D A1 Raskind, Wendy H A1 Schwake, Michael A1 Duvet, Sandrine A1 Foulquier, Francois A1 Matthijs, Gert A1 Marquardt, Thorsten A1 Simons, Matias PB eScholarship, University of California YR 2017 K1 Liver Disease K1 Digestive Diseases K1 Rare Diseases K1 2.1 Biological and endogenous factors K1 Aetiology K1 Adolescent K1 Amino Acid Sequence K1 Animals K1 Autophagy K1 Base Sequence K1 Blood Proteins K1 Brain K1 Cutis Laxa K1 Drosophila Proteins K1 Drosophila melanogaster K1 Endoplasmic Reticulum-Associated Degradation K1 Fibroblasts K1 Genes K1 X-Linked K1 Glycosylation K1 Humans K1 Infant K1 Lipids K1 Liver K1 Liver Diseases K1 Male K1 Membrane Proteins K1 Mice K1 Mutation K1 Neural Stem Cells K1 Protein Binding K1 Protein Processing K1 Post-Translational K1 Proton-Translocating ATPases K1 Psychomotor Disorders K1 Receptors K1 Cell Surface K1 Vacuolar Proton-Translocating ATPases K1 Young Adult K1 Medical and Health Sciences K1 Immunology JF qt8001g5w8 LK http://dx.doi.org/https://escholarship.org/uc/item/8001g5w8 DO https://escholarship.org/uc/item/8001g5w8 SF ELIB - SuUB Bremen
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