Nesrine Kerkeni
2PUBLICATIONS
5CO-AUTHORS
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Publications (2)
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|Jan 20, 2026
First Detection of 1p36 Deletion by Whole-Exome Sequencing in a Tunisian Patient.Nesrine Kerkeni, Maher Kharrat, Lilia Kraoua
|Feb 23, 2022
Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome.Nesrine Kerkeni, Maher Kharrat, Faouzi Maazoul
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