Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile.
| Autor: | Kindil, Zineb1,2, Senhaji, Mohamed Amine1, Bakhchane, Amina1, Charoute, Hicham1, Chihab, Soumia3, Nadifi, Sellama2, Barakat, Abdelhamid1 hamid.barakat@pasteur.ma |
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| Zdroj: | BMC Research Notes. 12/6/2017, Vol. 10, p1-6. 6p. 2 Diagrams, 3 Charts. |
| Databáze: | Academic Search Ultimate |
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