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Publications by Abdulaziz Al Hadlaq

Congenital Stationary Night Blindness With Hypoplastic Discs, Negative Electroretinogram and Thinning of the Inner Nuclear Layer

Graefe's Archive for Clinical and Experimental Ophthalmology

Molecular Neuroscience

Sensory Systems

English

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Congenital Stationary Night Blindness

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Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children

JAMA Ophthalmology

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Cav1.4 IT Mouse as Model for Vision Impairment in Human Congenital Stationary Night Blindness Type 2

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

American Journal of Human Genetics

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A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

BioMed Research International

Molecular Biology

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Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse

Multidisciplinary

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Chondroectodermal Dysplasia With Night Blindness

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Night-Blindness

British Journal of Ophthalmology

Molecular Neuroscience

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Night-Blindness and Vitamin A

English