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PLoS ONE, ISSN 1932-6203, 10/2015, Volume 10, Issue 10, p. e0139557
Journal Article
FEBS Journal, ISSN 1742-464X, 12/2006, Volume 273, Issue 23, pp. 5374 - 5383
Journal Article
FASEB Journal, ISSN 0892-6638, 11/2012, Volume 26, Issue 11, pp. 4468 - 4480
Journal Article
The EMBO Journal, ISSN 0261-4189, 12/2018, Volume 37, Issue 23, p. n/a
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2019, Volume 179, Issue 8, pp. 1580 - 1584
Infantile hereditary lower motor neuron disorders beyond 5q–spinal muscular atrophy (5q‐SMA) are usually caused by mutations other than deletions or mutations... 
AGTPBP1 | non‐5q spinal muscular atrophy | infantile neurodegeneration | cerebellar atrophy | cytosolic carboxypeptidase 1 | non-5q spinal muscular atrophy | GENETICS & HEREDITY | Physiological aspects | Neurons | Hypoplasia | Cerebellum | Atrophy | Phenotypes | Neurodegeneration | SMN protein | Carboxypeptidase | Children | Mutation | Spinal muscular atrophy
Journal Article
Molecular Biology of the Cell, ISSN 1059-1524, 10/2017, Volume 28, Issue 20, pp. 2686 - 2700
Extended coiled-coil proteins of the golgin family play prominent roles in maintaining the structure and function of the Golgi complex. Here we further... 
CARBOXYPEPTIDASE-Y | PURIFIED CYTOSOLIC PROTEINS | GENE DISRUPTION | MEMBRANE-PROTEIN | GLOBAL ANALYSIS | ENDOPLASMIC-RETICULUM | VESICLE DOCKING | YEAST SECRETORY PATHWAY | SACCHAROMYCES-CEREVISIAE | TETHERING COMPLEX | CELL BIOLOGY
Journal Article