Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome

American Journal of Human Genetics

Volumn 68, Issue 4, 2001, Pages 848-858

  Petek, Erwin ^a,b   Windpassinger, Christian ^a   Vincent, John B ^b   Cheung, Joseph ^b   Boright, Andrew P ^b   Scherer, Stephen W ^b   Kroisel, Peter M ^a   Wagner, Klaus ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PEPTIDASE; PROTEIN IMMP2L; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 7Q; CHROMOSOME DUPLICATION; DNA SEQUENCE; GENE DISRUPTION; GILLES DE LA TOURETTE SYNDROME; HUMAN; HUMAN CELL; LANGUAGE DISABILITY; MALE; MOLECULAR CLONING; NEUROPSYCHIATRY; PRIORITY JOURNAL; SPEECH DISORDER; TIC;

BACTERIA (MICROORGANISMS);

EID: 0035072652     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/319523     Document Type: Article

References (25)

1. The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: A large scale study
2. Current status of genetic studies of Gilles de la Tourette syndrome
3. Tourette syndrome in a pedigree with a 7;18 translocation: Identification of a YAC spanning the translocation breakpoint at 18q22.3
4. A prospective longitudinal study of Gilles de la Tourette's syndrome
5. Autosomal dominant gene transmission in a large kindred with Gilles de la Tourette syndrome
6. Signal peptidases in prokaryotes and eukaryotes: A new protease family
7. Gene location in Tourette syndrome
8. An international perspective on Tourette syndrome: Selected findings from 3,500 individuals in 22 countries
9. Recent developments in the molecular genetics of mitochondrial disorders
10. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
11. A decrease of reelin expression as a putative vulnerability factor in schizophrenia
12. Candidate region for Gilles de la Tourette syndrome at 7q31
13. The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
14. Mitochondrial respiratory chain disorders II: Neurodegenerative disorders and nuclear gene defects
15. Chromosome 7q22-q31 duplication: Report of a new case and review
16. Significant linkage for Tourette syndrome in a large French Canadian family
17. A mitochondrial protease with two catalytic subunits of nonoverlapping specificities
18. Isolation of site-specific insert probes from chimeric YACs
19. Annotation: Gilles de la Tourette syndrome: An update
20. Cloning, sequencing and localization to chromosome 11 of a cDNA encoding a human opioid-binding cell adhesion molecule (OBCAM)
21. Cloning and expression of a novel gene for a protein with leucine-rich repeats in the developing mouse nervous system
22. Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
23. Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual
24. Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31
25. Mitochondrial involvement in schizophrenia and other functional psychoses