1. Computational analysis of damaging nsSNP in human STXBP1 gene involved in early infantile epileptic encephalopathy: Molecular modelling and dynamics study. (September 2019) Authors: Krami, Al Mehdi; Roky, Rachida; Barakat, Abdelhamid; Nahili, Halima Journal: IBRO reports Issue: Volume 6(2019)Supplement Page Start: S410 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study. (26th July 2020) Authors: Ait El Cadi, Chaimaa; Krami, Al Mehdi; Charoute, Hicham; Elkarhat, Zouhair; Sifeddine, Najat; Lakhiari, Hamid; Rouba, Hassan; Barakat, Abdelhamid; Nahili, Halima Other Names: Evstigneev Maxim P. Academic Editor. Journal: BioMed research international Issue: Volume 2020(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome. (October 2018) Authors: Elrharchi, Soukaina; Riahi, Zied; Salime, Sara; Nahili, Halima; Rouba, Hassan; Kabine, Mostafa; Bonnet, Crystel; Petit, Christine; Barakat, Abdelhamid Journal: International journal of pediatric otorhinolaryngology Issue: Volume 113(2018:Oct.) Page Start: 46 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗