Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis. [electronic resource]
Producer: 20150922Description: 1106-18 p. digitalISSN:- 1460-2083
- Adult
- Child
- Child, Preschool
- DNA Mutational Analysis
- Exons
- Female
- Humans
- Intellectual Disability -- genetics
- Interleukin-1 Receptor Accessory Protein -- chemistry
- Introns
- Male
- Mutation
- Neurogenesis -- genetics
- Pedigree
- Polymorphism, Single Nucleotide
- Protein Interaction Domains and Motifs
- Protein Transport
- Sequence Deletion
- Signal Transduction
- Synapses -- genetics
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.