Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11–q13
Human chromosome 15q11–q13 is subject to regulation by genomic imprinting, an epigenetic process by which genes are expressed in a parent-of-origin specific manner. Three neurodevelopmental disorders, Prader–Willi syndrome, Angelman syndrome, and 15q duplication syndrome, result from aberrant expres...
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| Hauptverfasser: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Elsevier
2010-07-01
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| Schriftenreihe: | Neurobiology of Disease |
| Schlagworte: | |
| Online-Zugang: | http://www.sciencedirect.com/science/article/pii/S0969996110000720 |
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