Variable Cardiac Involvement in Tunisian Siblings Harboring FKRP Gene Mutations

Nasu-Hakola disease in two Tunisian siblings: new radiological findings

CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia.

International audience Primary congenital glaucoma (PCG) is responsible for a signifi

FANCA Gene Mutations in North African Fanconi Anemia Patients

Populations in North Africa (NA) are characterized by a high rate of consanguinity. Consequently, th

Implication of exon 4 TP53 Gene mutations in colorectal cancers in Senegalese patients

Background: Colorectal cancer (CRC) is a major cause of death in men and women, comprising about 10%

Spatiotemporal mathematical modelling of mutations of the dhps gene in African Plasmodium falciparum.

BACKGROUND: Plasmodium falciparum has repeatedly evolved resistance to first-line anti-malarial drug

Gene frequencies of human platelet antigens in the Tunisian population

Abstract: Gene frequencies for the human platelet antigens HPA‐1, ‐3 and ‐5 in the Tunisian populat