Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism. [electronic resource]
Producer: 20070202Description: 1073-84 p. digitalISSN:- 1359-4184
- Amino Acid Substitution
- Animals
- Autistic Disorder -- genetics
- Chromosomes, Human, X
- Female
- Hippocampus -- metabolism
- Humans
- Male
- X-Linked Intellectual Disability -- genetics
- Mice
- Models, Neurological
- Mutation, Missense
- Pedigree
- Protein Biosynthesis -- genetics
- Ribosomal Protein L10
- Ribosomal Proteins -- genetics
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Publication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
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