Mayssa Abdelwahed
3PUBLICATIONS
0CO-AUTHORS
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Publications (3)
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|May 31, 2020
Detection of a novel mutation in a Tunisian child with polycystic kidney disease.Mayssa Abdelwahed, Pascale Hilbert, Asma Ahmed
|Aug 13, 2019
Copy-number variation of the NPHP1 gene in patients with juvenile Nephronophthisis.Mayssa Abdelwahed, Ines Maaloul, Valerie Benoit
|Jul 19, 2019
A novel de novo splicing mutation c.1444-2A>T in the TSC2 gene causes exon skipping and premature termination in a patient with tuberous sclerosis syndrome.Mayssa Abdelwahed, Renaud Touraine, Bochra Ben-Rhouma
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