New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation

一个新发现的阿拉伯家庭患有脑发育不全、神经病变、鱼鳞病和角化过度综合征，这提示c.223delG突变可能存在创始人效应。