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1. Dihydrolipoamide dehydrogenase deficiency in two unrelated Tunisian children.

2. Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

6. Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

8. Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

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