1. Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis. (5th April 2013) Authors: M'hamdi, O.; Redin, C.; Stoetzel, C.; Ouertani, I.; Chaabouni, M.; Maazoul, F.; M'rad, R.; Mandel, J.L.; Dollfus, H.; Muller, J.; Chaabouni, H. Journal: Clinical genetics Issue: Volume 85:Number 2(2014:Feb.) Page Start: 172 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. SQSTM1 mutation: Description of the first Tunisian case and literature review. Issue 12 (2nd November 2020) Authors: Akkari, M.; Kraoua, I.; Klaa, H.; Benrhouma, H.; Ben Younes, T.; Rouissi, A.; Chaabouni, M.; Ben Youssef‐Turki, I. Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 12(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗