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Mutations in the X-linked ATP6AP2 cause a glycosylation dis..:
Rujano, Maria A
;
Cannata Serio, Magda
;
Panasyuk, Ganna
...
info:eu-repo/semantics/altIdentifier/doi/10.1084/jem.20170453. , 2017
Link:
https://hal.univ-lille.fr/hal-03273631
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-ftunivparis:oai:HAL:hal-03273631v1&Exemplar=1&LAN=DE A1 Rujano, Maria A A1 Cannata Serio, Magda 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 HAL CCSD YR 2017 K1 Young Adult K1 Genes K1 X-Linked K1 Base Sequence K1 Fibroblasts K1 Vacuolar Proton-Translocating ATPases K1 Amino Acid Sequence K1 Drosophila Proteins K1 Glycosylation K1 Neural Stem Cells K1 Animals K1 Blood Proteins K1 Proton-Translocating ATPases K1 Adolescent K1 Protein Binding K1 Mice K1 Membrane Protein K1 Protein Processing K1 Post-Translational K1 Mutation K1 Liver Diseases K1 Drosophila melanogaster K1 Psychomotor Disorders K1 Endoplasmic Reticulum-Associated Degradation K1 Brain K1 Humans K1 Liver K1 Cutis Laxa K1 Male K1 Lipids K1 Infant K1 Receptors K1 Cell Surface K1 Autophagy K1 [CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry JF info:eu-repo/semantics/altIdentifier/doi/10.1084/jem.20170453 LK http://dx.doi.org/https://hal.univ-lille.fr/hal-03273631 DO https://hal.univ-lille.fr/hal-03273631 SF ELIB - SuUB Bremen
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