Publications by authors named "Mohammad Mahroum"

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Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.
Rauan Kaiyrzhanov, Aboulfazl Rad, Sheng-Jia Lin, Aida Bertoli-Avella, Wouter W Kallemeijn, Mohammad Mahroum

Brain· April 2024

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[IDENTIFICATION OF A NOVEL LTBP3 GENE PATHOGENIC VARIANT IN DRUZE ARAB PATIENTS PRESENTED WITH SYNDROMIC SHORT STATURE WITH BRACHYOLMIA AND AMELOGENESIS IMPERFECTA].
Yarin Hadid, Ziad Daher, Mohammad Mahroum, Anan Shalata, Yara Nakhleh Francis

Harefuah· June 2023

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Primary Coenzyme Q deficiency Due to Novel ADCK3 Variants, Studies in Fibroblasts and Review of Literature.
Adel Shalata, Michael Edery, Clair Habib, Jacob Genizi, Mohammad Mahroum

Neurochem Res· October 2019

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