Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
暂无分享,去创建一个
B. Sharrack | Bareqa Salah | A. Awidi | B. Azab | Dema Ali | N. Ababneh | Malik Sallam | B. Al-Kurdi | A. T. Ryalat | Abdulla M Alzibdeh | A. Ryalat