L. El Matri

Consanguinity, endogamy, and genetic disorders in Tunisia

Nizar Ben Halim, Nissaf Ben Alaya, Lilia Romdhane et al. · Journal of Community Genetics · 2012 · 107 citations · Full text

Mendelian Disorder, Genetic Disorder, Global Health +3

Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy

Zhaoxia Ren, Pei-Yu Lin, Gordon K. Klintworth et al. · Human Genetics · 2002 · 98 citations · Full text

Ophthalmology, Corneal Dystrophy, Genetic Disorder +4

Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease

Andreas Gal, Isabella Rau, L. El Matri et al. · The American Journal of Human Genetics · 2011 · 92 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +5

Pediatric Penetrating Keratoplasty: Indications and Outcomes

R. Limaiem, A. Chebil, A. Baba et al. · Transplantation Proceedings · 2011 · 63 citations

Pediatric Surgery, Surgery, Wound Healing +2

Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene

L. El Matri, Aude Ambresin, Daniel F. Schorderet et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2006 · 42 citations · Full text

Consanguineous Tunisian Families, Rpe65 Gene, Retina +8