Whole-Exome Sequencing Revealed Mutations of MED12 and EFNB1 in Fetal Agenesis of the Corpus Callosum

Agenesis of the corpus callosum (ACC) is a birth defect in which the corpus callosum is either partially or completely missing. With recent advances in prenatal ultrasound, detection of ACC in obstetric practices is becoming more common. Etiologies of ACC include chromosome errors, genetic factors,...

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Dades bibliogràfiques
Publicat a:Front Genet
Autors principals: Jiang, Ying, Qian, Ye-Qing, Yang, Meng-Meng, Zhan, Qi-Tao, Chen, Yuan, Xi, Fang-Fang, Sagnelli, Matthew, Dong, Min-Yue, Zhao, Bai-Hui, Luo, Qiong
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2019
Matèries:
Genetics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6886535/
https://ncbi.nlm.nih.gov/pubmed/31824579
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.01201
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