Publications by authors named "Mohammed Mahroum"

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Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotype.
Adel Shalata, Ann Saada, Mohammed Mahroum, Yarin Hadid, Chaya Furman

Hum Genomics· February 2025

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Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and blood.
Adel Shalata, Supanun Lauhasurayotin, Zvi Leibovitz, Hongbing Li, Diane Hebert, Mohammed Mahroum

J Med Genet· May 2019

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Homothorax plays autonomous and nonautonomous roles in proximodistal axis formation and migration of the Drosophila renal tubules.
Adi Zohar-Stoopel, Nitzan Gonen, Mohammed Mahroum, Doreen S Ben-Zvi, Hila Toledano

Dev Dyn· January 2014

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Morbid obesity resulting from inactivation of the ciliary protein CEP19 in humans and mice.
Adel Shalata, Maria C Ramirez, Robert J Desnick, Nolan Priedigkeit, Christoph Buettner, Mohammed Mahroum

Am J Hum Genet· December 2013

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