Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile

por Kindil, Zineb, Senhaji, Mohamed Amine, Bakhchane, Amina, Charoute, Hicham, Chihab, Soumia, Nadifi, Sellama, Barakat, Abdelhamid
Publicado 2017