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Additional file 1: FigureS1. of Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia

Authors :
Bettencourt, Conceição
Salpietro, Vincenzo
Efthymiou, Stephanie
Chelban, Viorica
Hughes, Deborah
Pittman, Alan
Federoff, Monica
Bourinaris, Thomas
Spilioti, Martha
Deretzi, Georgia
Kalantzakou, Triantafyllia
Houlden, Henry
Singleton, Andrew
Xiromerisiou, Georgia
Publication Year :
2017
Publisher :
Figshare, 2017.

Abstract

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)

Subjects

Subjects :
nervous system

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....6b05ebcd66a9f80bb912399d8c452d56
Full Text :
https://doi.org/10.6084/m9.figshare.c.3920938_d1.v1