Prader-Willi syndrome (PWS) is a neuroendocrine genetic disorder resulting from the loss of paternally expressed imprinted genes in chromosome 15q11-q13 [...].
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381011 | PMC |
| http://dx.doi.org/10.3390/ijms241411574 | DOI Listing |
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