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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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4732947/
https://ncbi.nlm.nih.gov/pubmed/26824232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0148155
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