Ravinder K. Chana
Leicester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 8 publications
Properdin Deficiency Impairs Phagocytosis and Enhances Injury at Kidney Repair Phase Post Ischemia-Reperfusion.
Journal: Frontiers in immunology
Published: April 20, 2021
Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health Service.
Journal: Clinical genetics
Published: March 02, 2016
Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variants.
Journal: Human mutation
Published: June 02, 2014
Clinical and molecular characteristics of childhood-onset Stargardt disease.
Journal: Ophthalmology
Published: March 04, 2014
ABCA4 gene screening by next-generation sequencing in a British cohort.
Journal: Investigative ophthalmology & visual science
Published: August 29, 2013
Retinal structure and function in achromatopsia: implications for gene therapy.
Journal: Ophthalmology
Published: April 13, 2013
Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.
Journal: American journal of ophthalmology
Published: April 09, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026