Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile
Crossref DOI link: https://0-doi-org.brum.beds.ac.uk/10.1186/s13104-017-3042-6
Published Online: 2017-12-06
Published Print: 2017-12
Update policy: https://0-doi-org.brum.beds.ac.uk/10.1007/springer_crossmark_policy
Kindil, Zineb
Senhaji, Mohamed Amine
Bakhchane, Amina
Charoute, Hicham
Chihab, Soumia
Nadifi, Sellama
Barakat, Abdelhamid