Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences. [electronic resource]
Producer: 20140321Description: e1003752 p. digitalISSN:- 1553-7404
- Alleles
- Animals
- Apnea -- genetics
- Brain -- metabolism
- Disease Models, Animal
- Epigenesis, Genetic -- genetics
- Gene Expression Regulation
- Genomic Imprinting
- Heterozygote
- Humans
- Mice
- Mice, Knockout
- Nerve Tissue Proteins -- genetics
- Nuclear Proteins -- genetics
- Prader-Willi Syndrome -- genetics
- Promoter Regions, Genetic
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.