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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/16479


    Title: A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings
    Authors: 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Wang, Wayseen
    Contributors: 生物科技學系
    Keywords: Array-CGH;22q13 deletion syndrome;Autism;Epilepsy;Atopic dermatitis;Immune system;SHANK3;NCAPH2;CYP2D6
    Date: 2010-09
    Issue Date: 2012-11-23 17:13:39 (UTC+8)
    Abstract: We report a 5-year-old boy with mental retardation, autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings, carrying a 7.9 Mb de novo deletion of chromosome 22q13.2→qter. This region contains the SHANK3, NCAPH2 and CYP2D6 genes which are associated with T-cell immune response. The present case provides evidence that 22q13 deletion syndrome may be associated with immune system dysfunction in addition to neuropsychiatric disorders.
    Relation: European Journal of Medical Genetics
    Appears in Collections:[生物科技學系] 期刊論文

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