Additional file 1: FigureS1. of Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia
- Conceição Bettencourt (635298)
- Vincenzo Salpietro (4569352)
- Stephanie Efthymiou (4569349)
- Viorica Chelban (4569337)
- Deborah Hughes (4569331)
- Alan Pittman (4569346)
- Monica Federoff (4569343)
- Thomas Bourinaris (4569334)
- Martha Spilioti (4569328)
- Georgia Deretzi (3636889)
- Triantafyllia Kalantzakou (4569340)
- Henry Houlden (110428)
- Andrew Singleton (23294)
- Georgia Xiromerisiou (377223)
Publication date
November 2017
DOIAbstract
Expression of the AP4M1 gene in several regions of the human brain throughout development and aging. Note the higher expression levels during fetal development (birth is marked with a vertical solid line). Data from the Human Brain Transcriptome (HBT) project ( http://hbatlas.org ). CBC - cerebellar cortex, MD - mediodorsal nucleus of the thalamus, STR - striatum, AMY - amygdala, HIP - hippocampus, and NCX – neocortex. (PDF 68 kb
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