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Oxytocin’s Regulation of Thermogenesis May Be the Link to Prader–Willi Syndrome
Prader–Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297258/ https://www.ncbi.nlm.nih.gov/pubmed/37367062 http://dx.doi.org/10.3390/cimb45060313 |