Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents

por Ababneh, Nidaa A., Ali, Dema, Al-Kurdi, Ban, Sallam, Malik, Alzibdeh, Abdulla M., Salah, Bareqa, Ryalat, Abdee T., Azab, Belal, Sharrack, Basil, Awidi, Abdalla
Publicado 2020