Nacim Louhichi

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

Chahnez Triki, Susana Quijano‐Roy, Pascale Richard et al. · Neurogenetics · 2004 · 83 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss

Emna Mkaouar‐Rebai, Abdelaziz Tlili, Saber Masmoudi et al. · Biochemical and Biophysical Research Communications · 2006 · 25 citations

Life Sciences, Genetics, Molecular Genetics +17

Cupressus sempervirens Essential Oil: Exploring the Antibacterial Multitarget Mechanisms, Chemcomputational Toxicity Prediction, and Safety Assessment in Zebrafish Embryos

Sarra Akermi, Slim Smaoui, Khaoula Elhadef et al. · Molecules · 2022 · 24 citations · Full text

Agriculture, Food Science, Toxicology +17

Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect

Nacim Louhichi, Moez Medhaffar, Ikhlass Hadjsalem et al. · Annals of Hematology · 2009 · 21 citations

Life Sciences, Genetics, Molecular Genetics +15

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients

Chahnez Triki, Nacim Louhichi, M Méziou et al. · Neuromuscular Disorders · 2002 · 19 citations

Medicine, Genetics, Molecular Genetics +13