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.
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
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  Data: A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.
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  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.
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  Data: <searchLink fieldCode="JN" term="%222985248R%22">Medicine</searchLink> [Medicine (Baltimore)] 2025 Nov 14; Vol. 104 (46), pp. e45836.
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  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
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        Value: 10.1097/MD.0000000000045836
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        Text: English
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              Text: 2025 Nov 14
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