The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain

Nature Genetics
Claire RougeulleMarc Lalande

Abstract

No abstract listed.

Citations

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Related Concepts

Brain
Chromosomes, Human, Pair 15
DNA Transposons
Chromosome Inversion
Ligase
Lymphoid Cells
Tissue Specificity
Transcription, Genetic
Out-of-Frame Deletion
Angelman Syndrome

Related Feeds

Angelman Syndrome

Angelman syndrome is a neurogenetic imprinting disorder caused by loss of the maternally inherited UBE3A gene and is characterized by generalized epilepsy, limited expressive speech, sleep dysfunction, and movement disorders. Here is the latest research.

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