Author:
Chen Shimeng,Xiong Juan,Chen Baiyu,Zhang Ciliu,Deng Xiaolu,He Fang,Yang Lifen,Chen Chen,Peng Jing,Yin Fei
Funder
National Key Research and Development Program of China
Guangxi Key Research and Development Program
Key Project of Research and Development Plan of Hunan Province
National Natural Science Foundation of China
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference56 articles.
1. Genetic heterogeneity in autism: From single gene to a pathway perspective;An;Neurosci. Biobehav. Rev.,2016
2. Unexplained Early Infantile Epileptic Encephalopathy in Han Chinese Children: Next-Generation Sequencing and Phenotype Enriching;Arafat;Sci. Rep.,2017
3. Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature;Balasubramanian;J. Med. Genet.,2017
4. Berg, A. T., Berkovic, S. F., Brodie, M. J., Buchhalter, J., Cross, J. H., Van Emde Boas, W., . . . Scheffer, I. E. (2010). Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009. Epilepsia, 51(4), 676–685. 10.1111/j.1528-1167.2010.02522.x.
5. Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3;Blazejewski;Front. Genet.,2018
Cited by
8 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献