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Publications by Osama Alsmadi

ND4L Gene Concurrent 10609T>C and 10663T>C Mutations Are Associated With Leber's Hereditary Optic Neuropathy in a Large Pedigree From Kuwait

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2014English

Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children

Frontiers in Genetics
GeneticsMolecular Medicine
2018English

Assessment of Coding Region Variants in Kuwaiti Population: Implications for Medical Genetics and Population Genomics

Scientific Reports
Multidisciplinary
2018English

Mitochondrial DNA D-Loop Sequencing Reveals Obesity Variants in an Arab Population

The Application of Clinical Genetics
Genetics
2019English

Salivary Glucose Concentration Exhibits Threshold Kinetics in Normal-Weight, Overweight, and Obese Children

Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Internal MedicinePharmacology
2014English

Syndromic Congenital Sensorineural Deafness, Microtia and Microdontia Resulting From a Novel Homoallelic Mutation in Fibroblast Growth Factor 3 (FGF3)

European Journal of Human Genetics
Genetics
2008English

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