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Article from 2 yrs ago which provides a clear, concise overview of the dysfunction of striatal medium spiny neurons (MSNs) due to mutations in the genes encoding key postsynaptic proteins, including GNAO1 https://t.co/FLJKyblNwX
770 followers
RT @JIMD_Editors: #openaccess Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms Abela & Kurian review…
1,021 followers
RT @JIMD_Editors: #openaccess Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms Abela & Kurian review…
3,491 followers
RT @JIMD_Editors: #openaccess Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms Abela & Kurian review…
650 followers
RT @JIMD_Editors: #openaccess Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms Abela & Kurian review…
1,227 followers
RT @JIMD_Editors: #openaccess Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms Abela & Kurian review…
3,491 followers
#openaccess Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms Abela & Kurian review the clinical presentation, genetic findings, and disease mechanisms that characterize postsynaptic movement disorders @ucl_discove
2,519 followers
Open Access UCL Research: Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms https://t.co/GznSJZagdU
528 followers
Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms. https://t.co/uyoc2HZZ3g