Prader-Willi Critical Region, a Non-Translated, Imprinted Central Regulator of Bone Mass: Possible Role in Skeletal Abnormalities in Prader-Willi Syndrome

Prader-Willi Syndrome (PWS), a maternally imprinted disorder and leading cause of obesity, is characterised by insatiable appetite, poor muscle development, cognitive impairment, endocrine disturbance, short stature and osteoporosis. A number of causative loci have been located within the imprinted...

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Detalles Bibliográficos
Autores principales: Khor, Ee-Cheng, Fanshawe, Bruce, Qi, Yue, Zolotukhin, Sergei, Kulkarni, Rishikesh N., Enriquez, Ronaldo F., Purtell, Louise, Lee, Nicola J., Wee, Natalie K., Croucher, Peter I., Campbell, Lesley, Herzog, Herbert, Baldock, Paul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732947/
https://www.ncbi.nlm.nih.gov/pubmed/26824232
http://dx.doi.org/10.1371/journal.pone.0148155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732947/
https://www.ncbi.nlm.nih.gov/pubmed/26824232
http://dx.doi.org/10.1371/journal.pone.0148155

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