A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report.

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Bibliographic Details
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
Description
ISSN:1536-5964
DOI:10.1097/MD.0000000000045836