A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.
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| Title: | A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report. |
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| Authors: | Cao GH; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China., Zhang AQ; Department of Obstetrics and Gynecology, Third Xiangya Hospital of Central South University, Changsha, China., Dong Y; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China., Fan LL; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China., Yin JY; Department of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China., Tang LL; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China., Li YL; Department of Reproductive Genetics, Hebei Provincial Clinical Medical Research Center for Birth Defects, Hebei General Hospital, Shijiazhuang, China. |
| Source: | Medicine [Medicine (Baltimore)] 2025 Nov 14; Vol. 104 (46), pp. e45836. |
| Publication Type: | Journal Article; Case Reports |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41239616 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Cao+GH%22">Cao GH</searchLink>; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China.<br /><searchLink fieldCode="AU" term="%22Zhang+AQ%22">Zhang AQ</searchLink>; Department of Obstetrics and Gynecology, Third Xiangya Hospital of Central South University, Changsha, China.<br /><searchLink fieldCode="AU" term="%22Dong+Y%22">Dong Y</searchLink>; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China.<br /><searchLink fieldCode="AU" term="%22Fan+LL%22">Fan LL</searchLink>; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China.<br /><searchLink fieldCode="AU" term="%22Yin+JY%22">Yin JY</searchLink>; Department of Anesthesiology, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.<br /><searchLink fieldCode="AU" term="%22Tang+LL%22">Tang LL</searchLink>; Department of Cell Biology, School of Life Sciences, Central South University, Changsha, China.<br /><searchLink fieldCode="AU" term="%22Li+YL%22">Li YL</searchLink>; Department of Reproductive Genetics, Hebei Provincial Clinical Medical Research Center for Birth Defects, Hebei General Hospital, Shijiazhuang, China. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%222985248R%22">Medicine</searchLink> [Medicine (Baltimore)] 2025 Nov 14; Vol. 104 (46), pp. e45836. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Case Reports – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>2985248R <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1536-5964 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200257974%22">00257974 </searchLink><i>NLM ISO Abbreviation: </i>Medicine (Baltimore) <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41239616 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1097/MD.0000000000045836 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e45836 Titles: – TitleFull: A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Cao GH – PersonEntity: Name: NameFull: Zhang AQ – PersonEntity: Name: NameFull: Dong Y – PersonEntity: Name: NameFull: Fan LL – PersonEntity: Name: NameFull: Yin JY – PersonEntity: Name: NameFull: Tang LL – PersonEntity: Name: NameFull: Li YL IsPartOfRelationships: – BibEntity: Dates: – D: 14 M: 11 Text: 2025 Nov 14 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1536-5964 Numbering: – Type: volume Value: 104 – Type: issue Value: 46 Titles: – TitleFull: Medicine Type: main |
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