Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome

por Kerkeni, Nesrine, Kharrat, Maher, Maazoul, Faouzi, Boudabous, Hela, M’rad, Ridha, Trabelsi, Mediha
Publicado 2022

Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation

por Chograni, Manèl, Chaabouni, Myriam, Mâazoul, Faouzi, Bouzid, Hedi, Kraiem, Abdelhafid, Chaabouni, Habiba B Bouhamed
Publicado 2011

Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant as...

por Kraoua, Lilia, Jaouadi, Hager, Allouche, Mohamed, Achour, Ahlem, Kaouther, Hakim, Ahmed, Habib Ben, Chaker, Lilia, Maazoul, Faouzi, Ouarda, Fatma, Zaffran, Stéphane, M'rad, Ridha
Publicado 2022

Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved

por Mezzi, Nessrine, Messaoud, Olfa, Mkaouar, Rahma, Zitouna, Nadia, Romdhane, Safa, Abdessalem, Ghaith, Charfeddine, Cherine, Maazoul, Faouzi, Ouerteni, Ines, Hamdi, Yosr, Zaouak, Anissa, Mrad, Ridha, Abdelhak, Sonia, Romdhane, Lilia
Publicado 2021