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A prospective randomized double-blind placebo-controlled trial among elderly Swedish citizens
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doi: 10.1016/j.cmet.2005.11.015 74 LiCLiuCNissimIChenJChenPDolibaNet al
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Prader-Willi syndrome appears through loss of the paternal allele of chromosome 15q11-q13 [8 ]and it is characterized by hypotonia in infants, followed by obesity and excessive eating after early childhood, associated with significant mental impairments [12, 58]
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10.7554/eLife.10727 Elife
