1.
Int J Mol Sci
; 24(14)2023 Jul 18.
Artículo
en Inglés
| MEDLINE
| ID: mdl-37511333
RESUMEN
Prader-Willi syndrome (PWS) is a neuroendocrine genetic disorder resulting from the loss of paternally expressed imprinted genes in chromosome 15q11-q13 [...].