You are viewing the site in preview mode

Skip to main content
Fig. 6 | Molecular Autism

Fig. 6

From: Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism

Fig. 6

Transcript levels of PHF21A in the brain and other human tissue as determined by RT-qPCR. a A higher PHF21A expression was detected in the adult brain compared to the heart, kidney, liver, lung, skeletal muscle, and lymphocytes. b PHF21A is abundantly expressed in the fetal brain. High levels of PHF21A transcripts were also detected in the cerebellum, occipital lobe, postcentral gyrus, insula, cortex, and hippocampus

Back to article page

Molecular Autism

ISSN: 2040-2392