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Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
The Prader-Willi syndrome (PWS) is a human imprinting disorder resulting from genomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15q11-q13. This genetic condition appears to be a contiguous gene syndrome caused by the loss of at least 2 of a number o...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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The Korean Society of Pediatric Endocrinology
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073158/ https://www.ncbi.nlm.nih.gov/pubmed/27777904 http://dx.doi.org/10.6065/apem.2016.21.3.126 |