Page last updated: 2024-09-03

y 27632 and Congenital Myasthenia

y 27632 has been researched along with Congenital Myasthenia in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cairns, G; Cordts, I; Cox, D; Hettwer, S; Lochmüller, H; O'Connor, E; Phan, V; Roos, A1

Other Studies

1 other study(ies) available for y 27632 and Congenital Myasthenia

ArticleYear
MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretion.
    Human molecular genetics, 2018, 04-15, Volume: 27, Issue:8

    Topics: Actin Cytoskeleton; Actins; Agrin; Amides; Animals; Cell Movement; Disease Models, Animal; Embryo, Nonmammalian; Enzyme Inhibitors; Gene Expression Regulation; Humans; Intermediate Filaments; Membrane Proteins; Mice; Motor Neurons; Muscle Weakness; Myasthenic Syndromes, Congenital; Myosins; Nerve Growth Factor; Neuromuscular Junction; Protein Transport; Pyridines; rho GTP-Binding Proteins; rhoA GTP-Binding Protein; Tubulin; Zebrafish

2018