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Cannabinoid modulation of amygdala reactivity to social signals of threat in humans.
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia.
Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2.
Lissencephaly and the molecular basis of neuronal migration.
De novo mutations in SIK1 cause a spectrum of developmental epilepsies.
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De novo mutations in SIK1 cause a spectrum of developmental epilepsies.
De novo mutations in SIK1 cause a spectrum of developmental epilepsies. Am J Hum Genet. 2015 Apr 02; 96(4):682-90.
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PubMed
subject areas
Age Factors
Autistic Disorder
Base Sequence
Child
DNA Primers
Electroencephalography
Histone Deacetylases
Humans
Immunohistochemistry
Infant
Infant, Newborn
Magnetic Resonance Imaging
Molecular Sequence Data
Mutation
Phosphorylation
Polymerase Chain Reaction
Spasms, Infantile
authors with profiles
William B. Dobyns