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UnknownGOSR2 Lys67Arg is associated with hypertension in whites.
Not available
S-EPMC4346180 | biostudies-literature
UnknownThe Genotypic and Phenotypic Spectrum of GOSR2 Mutations: Clinical and Pathophysiological Insights.
Not available
S-EPMC12631098 | biostudies-literature
UnknownNovel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy.
Not available
S-EPMC10606070 | biostudies-literature
UnknownExpanding the Phenotype and Genetic Defects Associated with the <i>GOSR2</i> Gene.
Not available
S-EPMC6178697 | biostudies-literature
UnknownMutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity.
Not available
S-EPMC5640804 | biostudies-literature
UnknownA mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia.
Not available
S-EPMC3146720 | biostudies-literature
UnknownFunctional assays for the assessment of the pathogenicity of variants of GOSR2, an ER-to-Golgi SNARE involved in progressive myoclonus epilepsies.
Not available
S-EPMC5769602 | biostudies-literature
UnknownG-T haplotype established by rs3785889-rs16941382 in GOSR2 gene is associated with coronary artery disease in Chinese Han population.
Not available
S-EPMC5669879 | biostudies-literature
TranscriptomicsExpression of candidate genes associated with congenital heart disease in adult human atrial and ventricular tissue
We have used single nuclei RNAseq technology to analyze the expression of four candidate genes (MACROD2, GOSR2, WNT3, MSX1) in right atria and interventicular samples of adult human hearts. We find a robust expression of MACROD2 in all adult cardiac cell types. In contrast, expression of GOSR2 could...
ORGANISM(S): Homo sapiens 
2022-09-30 | GSE161016 | GEO
UnknownCortical Myoclonus in a Young Boy with GOSR2 Mutation Mimics Chorea.
Not available
S-EPMC6353358 | biostudies-literature
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