8650 Co-Localization Pattern of Snhg14 Long Noncoding RNA and Nhlh2 mRNA in Hypothalamus Coincides with Obesity and Endocrine Impairment Phenotypes in Prader-Willi Syndrome

• Published in: Journal of the Endocrine Society Vol. 8; no. Supplement_1
• Main Authors: Ariyanfar, Shadi, Thompson, Christopher K, Tobet, Stuart, Good, Deborah J
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 05.10.2024
• Subjects: Abstract

Abstract Disclosure: S. Ariyanfar: None. C.K. Thompson: None. S. Tobet: None. D.J. Good: None. Prader–Willi syndrome (PWS) is a multisystemic neurodevelopmental disorder, characterized by biphasic symptoms, including diminished weight gain during development, along with neonatal hypotonia and failur...