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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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Hlavní autoři: Skryabin, Boris V, Gubar, Leonid V, Seeger, Birte, Pfeiffer, Jana, Handel, Sergej, Robeck, Thomas, Karpova, Elena, Rozhdestvensky, Timofey S, Brosius, Jürgen
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2007
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On-line přístup: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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