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An Unexpected Function of the Prader-Willi Syndrome Imprinting Center in Maternal Imprinting in Mice
Genomic imprinting is a phenomenon that some genes are expressed differentially according to the parent of origin. Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are neurobehavioral disorders caused by deficiency of imprinted gene expression from paternal and maternal chromosome 15q11–q13, r...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3319576/ https://ncbi.nlm.nih.gov/pubmed/22496793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0034348 |
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