Spectrum of genetic variants in bilateral sensorineural hearing loss
Amanat Ali(United Arab Emirates University), Hiba Alblooshi(United Arab Emirates University), Mohammed Tabouni(United Arab Emirates University), Ibrahim Baydoun(École Normale Supérieure Paris-Saclay), Mushal Allam(United Arab Emirates University), Faiza Busafared(Dubai Hospital), Ayesha Alnuaimi(Dubai Hospital), Fatma Al‐Jasmi(United Arab Emirates University), Anne John(United Arab Emirates University), Praseetha Kizhakkedath(Institut thématique Génétique, génomique et bioinformatique)
Cited by 8
Related Papers
Higher education students’ perceptions of ChatGPT: A global study of early reactions
|PLoS ONE|2025|193
Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemia
|FEBS Open Bio|2019|53
Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies
|Molecular Genetics and Metabolism|2018|50
Utility of clinical exome sequencing in a complex Emirati pediatric cohort
|Computational and Structural Biotechnology Journal|2020|35