نتائج البحث - Michael Popiolek
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Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy حسب Christine P. Diggle, Stacey J. Sukoff Rizzo, Michael Popiolek, Reetta Hinttala, Jan-Philip Schülke, Manju A. Kurian, Ian Carr, Alexander F. Markham, David T. Bonthron, Christopher M. Watson, Saghira Malik Sharif, Veronica Reinhart, Larry C. James, Michelle Vanase‐Frawley, Erik I. Charych, Melanie Allen, John F. Harms, Christopher J. Schmidt, Joanne Ng, Karen Pysden, Christine A. Strick, Päivi Vieira, Katariina Mankinen, Hannaleena Kokkonen, Matti Kallioinen, Raija Sormunen, Juha O. Rinne, Jarkko Johansson, Kati Alakurtti, Laura Huilaja, Tiina Hurskainen, Kaisa Tasanen, Eija Anttila, Tiago Reis Marques, Oliver Howes, Marius Politis, Somayyeh Fahiminiya, Khanh Q. Nguyen, Jacek Majewski, Johanna Uusimaa, Eamonn Sheridan, Nicholas J. Brandon
منشور في 2016Artigo
أدوات البحث:
موضوعات ذات صلة
Biochemistry
Biology
Aesthetics
Chemistry
Disease
Entorhinal cortex
Enzyme
Excitatory postsynaptic potential
Glutamate receptor
Glutamatergic
Hippocampal formation
Hippocampus
Inhibitory postsynaptic potential
Internal medicine
Medicine
Movement (music)
Movement disorders
Muscarinic acetylcholine receptor
Neuroscience
Neurotransmission
PDE10A
Pediatrics
Philosophy
Phosphodiesterase
Psychology
Receptor
Schaffer collateral