Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairmentRahma Mkaouar, Médiha Trabelsi, Crystel Bonnet et al.|PLoS ONE|2021Cited by 5
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthRahma Mkaouar, Chérine Charfeddine, Zied Riahi et al.|Frontiers in Genetics|2024Cited by 1
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthRahma Mkaouar, Chérine Charfeddine, Zied Riahi et al.|Frontiers in Genetics|2024Cited by 1