The Role of Mitochondria in Prader–Willi Syndrome
Jul 14, 2025 · 5 min read · 1. Introduction Prader–Willi Syndrome (PWS) is a rare genetic disorder resulting from the lack of expression of paternally inherited genes in the 15q11–q13 chromosomal region. Clinically, it is characterized by neonatal hypotonia, hyperphagia, obesit...
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