Abdelbasset Amara

Genetics of low spinal muscular atrophy carrier frequency in sub‐Saharan Africa

Modibo Sangaré, Brant C. Hendrickson, Hammadoun Aly Sango et al. · Annals of Neurology · 2014 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients

Abdelbasset Amara, Labiba Adala, Ilhem Ben Charfeddine et al. · European Journal of Paediatric Neurology · 2011 · 39 citations

Life Sciences, Genetics, Molecular Genetics +11

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III

A. Mili, Ilhem Ben Charfeddine, Ons Mamaï et al. · Journal of Human Genetics · 2011 · 27 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +13

Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family

Ilhem Ben Charfeddine, Felix G. Riepe, N. Kahloul et al. · General and Comparative Endocrinology · 2011 · 23 citations

Life Sciences, Endocrinology, Genetics +17

Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population

Houda Ghédir, Moez Gribaa, Ons Mamaï et al. · Journal of Assisted Reproduction and Genetics · 2015 · 21 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15