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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Detalles Bibliográficos
Autores principales: Skryabin, Boris V, Gubar, Leonid V, Seeger, Birte, Pfeiffer, Jana, Handel, Sergej, Robeck, Thomas, Karpova, Elena, Rozhdestvensky, Timofey S, Brosius, Jürgen
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323313/
https://www.ncbi.nlm.nih.gov/pubmed/18166085
http://dx.doi.org/10.1371/journal.pgen.0030235

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323313/
https://www.ncbi.nlm.nih.gov/pubmed/18166085
http://dx.doi.org/10.1371/journal.pgen.0030235

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