Novel de novo SHANK3 mutation in autistic patients. [electronic resource]
Producer: 20090519Description: 421-4 p. digitalISSN:- 1552-485X
- Amino Acid Sequence
- Amino Acid Substitution
- Autistic Disorder -- genetics
- Carrier Proteins -- genetics
- Case-Control Studies
- Cohort Studies
- DNA Mutational Analysis
- Genetic Markers
- Humans
- Introns
- Male
- Microsatellite Repeats
- Molecular Sequence Data
- Mutation -- genetics
- Mutation, Missense
- Nerve Tissue Proteins
- Phenotype
- Proline -- metabolism
- RNA Splice Sites
- Sequence Deletion
- Sequence Homology, Amino Acid
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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