Identification of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing
Identi?cation of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing作者机构:Shanghai Mental Health CenterShanghai Jiao Tong University School of MedicineShanghai 200030China Institute of NeuroscienceCenter for Excellence in BrainScience and Intelligence TechnologyShanghai Institutes for Biological SciencesChinese Academy of SciencesShanghai 200031China School of Life SciencesPeking UniversityBeijing 100871China Euler GenomicsBeijing 102206China
出 版 物:《Neuroscience Bulletin》 (神经科学通报(英文版))
年 卷 期:2017年第33卷第2期
页 面:251-254页
核心收录:
学科分类:1002[医学-临床医学] 100205[医学-精神病与精神卫生学] 10[医学]
基 金:supported by the Chinese Academy of Sciences Strategic Priority Research Program,China(XDB02050400) the National Natural Science Foundation of China(91432111) the Shanghai Second Medical University-Institute of Neuroscience Research Center for Brain Disorders,China(2015NKX005)
主 题:Identi?cation of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing IIIA CDD
摘 要:Dear Editor,Childhood Disintegrative Disorder(CDD),also known as Heller’s syndrome and disintegrative psychosis,is a rare progressive neurological disorder,characterized by a late onset([2 years of age)and regression of language,social