Mohammed A Al-Muhaizea

6PUBLICATIONS
30CO-AUTHORS
Cell and nuclear divisionDental therapeutics, pharmacology and toxicologyCellular nervous systemNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (6)

|Aug 13, 2026
A Novel SLC25A4 Variant Causing Mitochondrial Dysfunction, Myopathy and Cardiomyopathy: A Functional and Molecular Characterization.

|Apr 14, 2026
Genetic, Clinical, and Management Characteristics of Duchenne Muscular Dystrophy in Saudi Arabia.

Abdulaziz S AlSaman, Fouad Al Ghamdi, Ahmed K Bamaga

|Jul 17, 2023
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission.

James Fasham, Antje K Huebner, Lutz Liebmann

|Nov 27, 2021
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population.

Mohammad AlMuhaizea, Omar Dabbagh, Hanan AlQudairy

|Aug 10, 2021
Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder.

Eva Medico Salsench, Reza Maroofian, Ruizhi Deng

|Sep 24, 2017
Molecular and clinical spectra of FBXL4 deficiency.

Ayman W El-Hattab, Hongzheng Dai, Mohammed Almannai

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Frequent Collaborators

3 joint publications

Namik Kaya

2 joint publications

Henry Houlden

2 joint publications

Dilek Colak

1 joint publications

James Fasham