Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice. [electronic resource]
Producer: 20160829Description: 643-52 p. digitalISSN:- 1537-6605
- Abnormalities, Multiple -- genetics
- Adult
- Alleles
- Amino Acid Sequence
- Animals
- Case-Control Studies
- Child
- Child, Preschool
- Codon, Nonsense
- Female
- Gene Expression Profiling
- Gene Expression Regulation
- Humans
- Intracellular Signaling Peptides and Proteins
- Male
- Mice
- Molecular Sequence Data
- Mutation
- Nonsense Mediated mRNA Decay -- genetics
- Pedigree
- Phosphoproteins -- genetics
- Phosphorylation
- Polymorphism, Single Nucleotide
- RNA, Messenger
- Saudi Arabia
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.