Llwytho...
Early Origin and Evolution of the Angelman Syndrome Ubiquitin Ligase Gene Ube3a
The human Ube3a gene encodes an E3 ubiquitin ligase and exhibits brain-specific genomic imprinting. Genetic abnormalities that affect the maternal copy of this gene cause the neurodevelopmental disorder Angelman syndrome (AS), which is characterized by severe mental retardation, speech impairment, s...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Front Cell Neurosci |
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| Prif Awdur: | |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Frontiers Media S.A.
2017
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5339648/ https://ncbi.nlm.nih.gov/pubmed/28326016 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2017.00062 |
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