Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q. [electronic resource]
Producer: 20091123Description: 817-26 p. digitalISSN:- 1552-485X
- Autistic Disorder -- genetics
- Base Sequence
- Chromosome Breakage
- Chromosomes, Human, Pair 18 -- genetics
- Chromosomes, Human, Pair 5 -- genetics
- DNA Mutational Analysis
- Desmocollins -- genetics
- Humans
- Intracellular Signaling Peptides and Proteins
- Male
- Molecular Sequence Data
- Multigene Family
- Polymorphism, Single Nucleotide
- Proteins -- genetics
- Receptors, Adrenergic, beta-2 -- genetics
- Receptors, Serotonin -- genetics
- Translocation, 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.