T. Kammoun

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome

Fakhri Kallabi, Neila Belghuith, Hajer Aloulou et al. · Archives of Medical Research · 2016 · 29 citations

Life Sciences, Genetics, Molecular Genetics +6

Association of TCR/CD3, PTPN22, CD28 and ZAP70 gene polymorphisms with type 1 diabetes risk in Tunisian population: Family based association study

Ferjeni Zouidi, Dorra Bouzid, H. Fourati et al. · Immunology Letters · 2014 · 25 citations

Medicine, Genetics, Molecular Genetics +15

Contribution of PTPN22, CD28, CTLA-4 and ZAP-70 variants to the risk of type 1 diabetes in Tunisians

Ferjeni Zouidi, Mouna Stayoussef, Dorra Bouzid et al. · Gene · 2013 · 20 citations

Medicine, Endocrinology, Immunology +11

A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNAIle m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss

Imen Chamkha, Emna Mkaouar‐Rebai, Hajer Aloulou et al. · Biochemical and Biophysical Research Communications · 2010 · 18 citations

Life Sciences, Genetics, Molecular Genetics +17

Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNATrp in patients with Leigh syndrome

Emna Mkaouar‐Rebai, Imen Chamkha, Fatma Kammoun et al. · Molecular Genetics and Metabolism · 2009 · 18 citations

Life Sciences, Genetics, Molecular Genetics +6