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Deletion of the MBII-85 snoRNA Gene Cluster in Mice Results in Postnatal Growth Retardation
Prader-Willi syndrome (PWS [MIM 176270]) is a neurogenetic disorder characterized by decreased fetal activity, muscular hypotonia, failure to thrive, short stature, obesity, mental retardation, and hypogonadotropic hypogonadism. It is caused by the loss of function of one or more imprinted, paternal...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2323313/ https://ncbi.nlm.nih.gov/pubmed/18166085 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.0030235 |
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