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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Detalles Bibliográficos
Autor principal: Camerino, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297258/
https://www.ncbi.nlm.nih.gov/pubmed/37367062
http://dx.doi.org/10.3390/cimb45060313

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