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- W4384695099 abstract "Prader-Willi syndrome (PWS) is a neuroendocrine genetic disorder resulting from the loss of paternally expressed imprinted genes in chromosome 15q11-q13 [...]." @default.
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- W4384695099 date "2023-07-18" @default.
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- W4384695099 title "The Arduous Path to Drug Approval for the Management of Prader–Willi Syndrome: A Historical Perspective and Call to Action" @default.
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- W4384695099 doi "https://doi.org/10.3390/ijms241411574" @default.
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