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

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About: Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	artículu científicu espublizáu en 2001 (ast) vědecký článek publikovaný v roce 2001 (cs) наукова стаття, опублікована у квітні 2001 (uk) 2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت في أبريل 2001) (ar) 2001 թվականի ապրիլին հրատարակված գիտական հոդված (hy) wetenschappelijk artikel (gepubliceerd op 2001/04/01) (nl) vedecký článok (publikovaný 2001/04/01) (sk) scientific journal article (en) im März 2001 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28587450-12227C4E-7567-48E3-9F48-822611CAB6B3
publication date	2001-03-09 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28587450-5B8B4CD2-6A6C-43ED-BD70-E36A13330667
language of work or name	English
cites work	wds:Q28587450-043022FE-30AF-4911-917D-A8F9805B8530 wds:Q28587450-0B872C07-E7F7-4E50-BBE0-D96459A55380 wds:Q28587450-139478D7-8891-4B1A-9148-3899E2C7A916 wds:Q28587450-19F3397F-90FC-46F6-9F1B-4788CBB0BA4B wds:Q28587450-1E0F0E15-AE97-41A6-AD1B-A771D6AD3D8B wds:Q28587450-2A0F745D-C4AA-4B71-B908-2CEA6A6461E3 wds:Q28587450-2C7D12A5-1AE4-4EE6-B0F6-832A932A26F5 wds:Q28587450-595E26B1-2E07-48DC-AAE4-17689FFBEA6D wds:Q28587450-5E64F33C-34F4-4EDA-B1BC-C8184114EF74 wds:Q28587450-60FBDB31-67EF-44CB-B297-8528C5990982 wds:Q28587450-6F1DB37A-924D-4B24-9123-F34284462B25 wds:Q28587450-803EA61A-391F-476A-B8BB-AC8466967AD6 wds:Q28587450-8B939DAF-16EE-4998-9D61-0673CB78CE6B wds:Q28587450-960DE7FB-AE5F-414A-BBBD-34C37396F1FD wds:Q28587450-A099C5E2-7779-42E4-8A85-38864820E36A wds:Q28587450-B1E77475-0E33-4ECF-AA05-AE8AF3671FBB wds:Q28587450-C1919881-6832-4F9D-8BA4-80FE88FD36AD wds:Q28587450-CC5E52A1-35C8-428A-822C-AC8BC417E701 wds:Q28587450-CEDF5333-BCAF-45EB-96E2-3E4B4234E9A3 wds:Q28587450-CF50E83F-AD2E-4ABF-BD9B-3F578D8E7057 wds:Q28587450-D43D049D-F9F5-4C29-9E27-78F09259FD28 wds:Q28587450-DC9B1B7C-88DF-4642-9252-A226BB795816 wds:Q28587450-E7473947-341F-4C22-93A6-13F16F3B1751 wds:Q28587450-F5372E2A-0C59-484A-A61E-5C8158C1D374 wds:Q28587450-F8ABBA53-5319-4640-A9E5-E62F56421D3C
cites work	The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries Cloning and expression of a novel gene for a protein with leucine-rich repeats in the developing mouse nervous system Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations A decrease of reelin expression as a putative vulnerability factor in schizophrenia Mitochondrial involvement in schizophrenia and other functional psychoses A mitochondrial protease with two catalytic subunits of nonoverlapping specificities. Signal peptidases in prokaryotes and eukaryotes--a new protease family Significant linkage for Tourette syndrome in a large French Canadian family The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: a large scale study A prospective longitudinal study of Gilles de la Tourette's syndrome. Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects Candidate region for Gilles de la Tourette syndrome at 7q31 Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31. Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3. Gene location in Tourette syndrome Annotation: Gilles de la Tourette syndrome--an update Cloning, sequencing and localization to chromosome 11 of a cDNA encoding a human opioid-binding cell adhesion molecule (OBCAM) Recent developments in the molecular genetics of mitochondrial disorders Isolation of site-specific insert probes from chimeric YACs Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual Current status of genetic studies of Gilles de la Tourette syndrome Chromosome 7q22-q31 duplication: report of a new case and review
author name string	wds:Q28587450-08DA2A4B-1EBA-44C4-A7E2-CFF0162928EE wds:Q28587450-63AD9887-7C81-462E-88A3-608B0D2682D6 wds:Q28587450-7C2628F8-418C-4E20-A304-4E670D3FD69A wds:Q28587450-813179C6-617F-4DB5-8A6E-4342BA71A88F wds:Q28587450-93590ADF-D64F-41C6-8004-E4798E596AFE wds:Q28587450-B5CA3D8A-618A-4E8C-9406-5B66A4F97157 wds:Q28587450-C7C262EB-A4A3-44BB-9AAB-93FF31E0F789
OpenCitations bibliographic resource ID	wds:Q28587450-1B2EE30B-5A95-4958-A15E-2B53038A0D8E
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/369448
author name string	Vincent JB Wagner K Cheung J Kroisel PM Petek E Windpassinger C Boright AP
OpenCitations bibliographic resource ID	369448
rdfs:label	Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (en) Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (nl) Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (ast)
skos:prefLabel	Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (en) Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (nl) Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (ast)
name	Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (en) Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (nl) Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (ast)
author	wds:Q28587450-DC8689FB-DFEE-421A-BE07-B990E848140A
author	Stephen W. Scherer
title	wds:Q28587450-FB46A311-81DE-4F4A-8087-EAFE8720351E
title	Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome (en)
page(s)	wds:Q28587450-E8D8CB9E-CB60-4AE0-BFFA-34F6653CE4A5
page(s)	848-858
instance of	wds:Q28587450-C72FFF15-6095-4016-8BDF-98EC9E209168
instance of	scholarly article
main subject	wds:Q28587450-10273455-ECB1-4570-AD4C-EFEFB915EA98

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