強度行動障害児(者)の処遇システムに関する研究 : 特別処遇事業の実践成果から
Published in 川崎医療福祉学会誌 • Jan 1, 1994
Authors:,,
好生 松本
洋子 中島
茂 末光
Abstract
Type I lissencephaly, a genetic disease characterized by disorganized cortical layers and gyral abnormalities, is associated with severe cognitive impairment and epilepsy. Two genes, LIS1 and doublecortin (DCX), have been shown to be responsible for a large proportion of cases of type I lissencephal...
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