Associated Papers
Expansion of genotypic and phenotypic findings in ADAMTS18-related ocular pathology.
August AH et al.
American Journal of Ophthalmology Case Reports, 2025
Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort.
Lin S et al.
Ophthalmology. Retina, 2024
38219857 (PubMed )
Supplement: mmc1.pdf
Genomic Landscape and Mutational Spectrum of ADAMTS Family Genes in Mendelian Disorders Based on Gene Evidence Review for Variant Interpretation.
Rim JH et al.
Biomolecules, 2020
Expansion of ocular phenotypic features associated with mutations in ADAMTS18.
Chandra A et al.
Jama Ophthalmology, 2014
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