High levels of LIGHT/TNFSF14 in patients with prader–willi syndrome
MF Faienza, G Brunetti, D Fintini, G Grugni… - Journal of …, 2023 - Springer
Abstract Purpose/methods Prader–Willi syndrome (PWS) is a rare genetic disorder
displaying different clinical features, including obesity and bone impairment …
displaying different clinical features, including obesity and bone impairment …